Name: rs34235841
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs34235841

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:51663595-51663618 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₃ / dup(A)₂₂ / ins(A)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₄=0.4980 (2494/5008, 1000G)
del(A)₁₄=0.000 (0/996, ALFA)
del(A)₁₃=0.000 (0/996, ALFA) (+ 12 more)
del(A)₁₂=0.000 (0/996, ALFA)
del(A)₁₁=0.000 (0/996, ALFA)
del(A)₁₀=0.000 (0/996, ALFA)
del(A)₈=0.000 (0/996, ALFA)
del(A)₇=0.000 (0/996, ALFA)
del(A)₆=0.000 (0/996, ALFA)
del(A)₅=0.000 (0/996, ALFA)
del(A)₄=0.000 (0/996, ALFA)
delAAA=0.000 (0/996, ALFA)
delAA=0.000 (0/996, ALFA)
delA=0.000 (0/996, ALFA)
dupA=0.000 (0/996, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAD54L2 : 3 Prime UTR Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	996	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	498	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	246	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	238	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	142	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	54	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₄=0.4980	delA=0.5020
1000Genomes	African	Sub	1322	(A)₂₄=0.6097	delA=0.3903
1000Genomes	East Asian	Sub	1008	(A)₂₄=0.4167	delA=0.5833
1000Genomes	Europe	Sub	1006	(A)₂₄=0.4195	delA=0.5805
1000Genomes	South Asian	Sub	978	(A)₂₄=0.584	delA=0.416
1000Genomes	American	Sub	694	(A)₂₄=0.396	delA=0.604
Allele Frequency Aggregator	Total	Global	996	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	European	Sub	498	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	African	Sub	246	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	142	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	54	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Asian	Sub	20	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.51663605_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663606_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663607_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663608_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663609_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663611_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663612_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663613_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663614_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663615_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663616_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663617_51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663618del
GRCh38.p14 chr 3	NC_000003.12:g.51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663617_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663616_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663615_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663612_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663611_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663610_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663609_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663608_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663606_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663597_51663618dup
GRCh38.p14 chr 3	NC_000003.12:g.51663618_51663619insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 3	NC_000003.11:g.51697621_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697622_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697623_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697624_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697625_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697627_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697628_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697629_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697630_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697631_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697632_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697633_51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697634del
GRCh37.p13 chr 3	NC_000003.11:g.51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697633_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697632_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697631_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697628_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697627_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697626_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697625_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697624_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697622_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697613_51697634dup
GRCh37.p13 chr 3	NC_000003.11:g.51697634_51697635insAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: RAD54L2, RAD54 like 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAD54L2 transcript variant 2	NM_015106.4:c.175_198=	N/A	3 Prime UTR Variant
RAD54L2 transcript variant 3	NM_001322256.2:c.175_19… NM_001322256.2:c.175_198=	N/A	3 Prime UTR Variant
RAD54L2 transcript variant 1	NM_001322253.2:c.175_19… NM_001322253.2:c.175_198=	N/A	3 Prime UTR Variant
RAD54L2 transcript variant 7	NM_001387869.1:c.175_19… NM_001387869.1:c.175_198=	N/A	3 Prime UTR Variant
RAD54L2 transcript variant 5	NM_001387866.1:c.175_19… NM_001387866.1:c.175_198=	N/A	3 Prime UTR Variant
RAD54L2 transcript variant 6	NM_001387867.1:c.175_19… NM_001387867.1:c.175_198=	N/A	3 Prime UTR Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₂₄=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₃	dup(A)₂₂	ins(A)₂₅
GRCh38.p14 chr 3	NC_000003.12:g.51663595_51663618=	NC_000003.12:g.51663605_51663618del	NC_000003.12:g.51663606_51663618del	NC_000003.12:g.51663607_51663618del	NC_000003.12:g.51663608_51663618del	NC_000003.12:g.51663609_51663618del	NC_000003.12:g.51663611_51663618del	NC_000003.12:g.51663612_51663618del	NC_000003.12:g.51663613_51663618del	NC_000003.12:g.51663614_51663618del	NC_000003.12:g.51663615_51663618del	NC_000003.12:g.51663616_51663618del	NC_000003.12:g.51663617_51663618del	NC_000003.12:g.51663618del	NC_000003.12:g.51663618dup	NC_000003.12:g.51663617_51663618dup	NC_000003.12:g.51663616_51663618dup	NC_000003.12:g.51663615_51663618dup	NC_000003.12:g.51663612_51663618dup	NC_000003.12:g.51663611_51663618dup	NC_000003.12:g.51663610_51663618dup	NC_000003.12:g.51663609_51663618dup	NC_000003.12:g.51663608_51663618dup	NC_000003.12:g.51663606_51663618dup	NC_000003.12:g.51663597_51663618dup	NC_000003.12:g.51663618_51663619insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 3	NC_000003.11:g.51697611_51697634=	NC_000003.11:g.51697621_51697634del	NC_000003.11:g.51697622_51697634del	NC_000003.11:g.51697623_51697634del	NC_000003.11:g.51697624_51697634del	NC_000003.11:g.51697625_51697634del	NC_000003.11:g.51697627_51697634del	NC_000003.11:g.51697628_51697634del	NC_000003.11:g.51697629_51697634del	NC_000003.11:g.51697630_51697634del	NC_000003.11:g.51697631_51697634del	NC_000003.11:g.51697632_51697634del	NC_000003.11:g.51697633_51697634del	NC_000003.11:g.51697634del	NC_000003.11:g.51697634dup	NC_000003.11:g.51697633_51697634dup	NC_000003.11:g.51697632_51697634dup	NC_000003.11:g.51697631_51697634dup	NC_000003.11:g.51697628_51697634dup	NC_000003.11:g.51697627_51697634dup	NC_000003.11:g.51697626_51697634dup	NC_000003.11:g.51697625_51697634dup	NC_000003.11:g.51697624_51697634dup	NC_000003.11:g.51697622_51697634dup	NC_000003.11:g.51697613_51697634dup	NC_000003.11:g.51697634_51697635insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 2	NM_015106.4:c.175_198=	NM_015106.4:c.185_198del	NM_015106.4:c.186_198del	NM_015106.4:c.187_198del	NM_015106.4:c.188_198del	NM_015106.4:c.189_198del	NM_015106.4:c.191_198del	NM_015106.4:c.192_198del	NM_015106.4:c.193_198del	NM_015106.4:c.194_198del	NM_015106.4:c.195_198del	NM_015106.4:c.196_198del	NM_015106.4:c.197_198del	NM_015106.4:c.*198del	NM_015106.4:c.*198dup	NM_015106.4:c.197_198dup	NM_015106.4:c.196_198dup	NM_015106.4:c.195_198dup	NM_015106.4:c.192_198dup	NM_015106.4:c.191_198dup	NM_015106.4:c.190_198dup	NM_015106.4:c.189_198dup	NM_015106.4:c.188_198dup	NM_015106.4:c.186_198dup	NM_015106.4:c.177_198dup	NM_015106.4:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 2	NM_015106.3:c.175_198=	NM_015106.3:c.185_198del	NM_015106.3:c.186_198del	NM_015106.3:c.187_198del	NM_015106.3:c.188_198del	NM_015106.3:c.189_198del	NM_015106.3:c.191_198del	NM_015106.3:c.192_198del	NM_015106.3:c.193_198del	NM_015106.3:c.194_198del	NM_015106.3:c.195_198del	NM_015106.3:c.196_198del	NM_015106.3:c.197_198del	NM_015106.3:c.*198del	NM_015106.3:c.*198dup	NM_015106.3:c.197_198dup	NM_015106.3:c.196_198dup	NM_015106.3:c.195_198dup	NM_015106.3:c.192_198dup	NM_015106.3:c.191_198dup	NM_015106.3:c.190_198dup	NM_015106.3:c.189_198dup	NM_015106.3:c.188_198dup	NM_015106.3:c.186_198dup	NM_015106.3:c.177_198dup	NM_015106.3:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript	NM_015106.2:c.175_202=	NM_015106.2:c.189_202del	NM_015106.2:c.190_202del	NM_015106.2:c.191_202del	NM_015106.2:c.192_202del	NM_015106.2:c.193_202del	NM_015106.2:c.195_202del	NM_015106.2:c.196_202del	NM_015106.2:c.197_202del	NM_015106.2:c.198_202del	NM_015106.2:c.199_202del	NM_015106.2:c.200_202del	NM_015106.2:c.201_202del	NM_015106.2:c.*202del	NM_015106.2:c.*202dup	NM_015106.2:c.201_202dup	NM_015106.2:c.200_202dup	NM_015106.2:c.199_202dup	NM_015106.2:c.196_202dup	NM_015106.2:c.195_202dup	NM_015106.2:c.194_202dup	NM_015106.2:c.193_202dup	NM_015106.2:c.192_202dup	NM_015106.2:c.190_202dup	NM_015106.2:c.181_202dup	NM_015106.2:c.178_202dup
RAD54L2 transcript variant 1	NM_001322253.2:c.175_198=	NM_001322253.2:c.185_198del	NM_001322253.2:c.186_198del	NM_001322253.2:c.187_198del	NM_001322253.2:c.188_198del	NM_001322253.2:c.189_198del	NM_001322253.2:c.191_198del	NM_001322253.2:c.192_198del	NM_001322253.2:c.193_198del	NM_001322253.2:c.194_198del	NM_001322253.2:c.195_198del	NM_001322253.2:c.196_198del	NM_001322253.2:c.197_198del	NM_001322253.2:c.*198del	NM_001322253.2:c.*198dup	NM_001322253.2:c.197_198dup	NM_001322253.2:c.196_198dup	NM_001322253.2:c.195_198dup	NM_001322253.2:c.192_198dup	NM_001322253.2:c.191_198dup	NM_001322253.2:c.190_198dup	NM_001322253.2:c.189_198dup	NM_001322253.2:c.188_198dup	NM_001322253.2:c.186_198dup	NM_001322253.2:c.177_198dup	NM_001322253.2:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 1	NM_001322253.1:c.175_198=	NM_001322253.1:c.185_198del	NM_001322253.1:c.186_198del	NM_001322253.1:c.187_198del	NM_001322253.1:c.188_198del	NM_001322253.1:c.189_198del	NM_001322253.1:c.191_198del	NM_001322253.1:c.192_198del	NM_001322253.1:c.193_198del	NM_001322253.1:c.194_198del	NM_001322253.1:c.195_198del	NM_001322253.1:c.196_198del	NM_001322253.1:c.197_198del	NM_001322253.1:c.*198del	NM_001322253.1:c.*198dup	NM_001322253.1:c.197_198dup	NM_001322253.1:c.196_198dup	NM_001322253.1:c.195_198dup	NM_001322253.1:c.192_198dup	NM_001322253.1:c.191_198dup	NM_001322253.1:c.190_198dup	NM_001322253.1:c.189_198dup	NM_001322253.1:c.188_198dup	NM_001322253.1:c.186_198dup	NM_001322253.1:c.177_198dup	NM_001322253.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 3	NM_001322256.2:c.175_198=	NM_001322256.2:c.185_198del	NM_001322256.2:c.186_198del	NM_001322256.2:c.187_198del	NM_001322256.2:c.188_198del	NM_001322256.2:c.189_198del	NM_001322256.2:c.191_198del	NM_001322256.2:c.192_198del	NM_001322256.2:c.193_198del	NM_001322256.2:c.194_198del	NM_001322256.2:c.195_198del	NM_001322256.2:c.196_198del	NM_001322256.2:c.197_198del	NM_001322256.2:c.*198del	NM_001322256.2:c.*198dup	NM_001322256.2:c.197_198dup	NM_001322256.2:c.196_198dup	NM_001322256.2:c.195_198dup	NM_001322256.2:c.192_198dup	NM_001322256.2:c.191_198dup	NM_001322256.2:c.190_198dup	NM_001322256.2:c.189_198dup	NM_001322256.2:c.188_198dup	NM_001322256.2:c.186_198dup	NM_001322256.2:c.177_198dup	NM_001322256.2:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 3	NM_001322256.1:c.175_198=	NM_001322256.1:c.185_198del	NM_001322256.1:c.186_198del	NM_001322256.1:c.187_198del	NM_001322256.1:c.188_198del	NM_001322256.1:c.189_198del	NM_001322256.1:c.191_198del	NM_001322256.1:c.192_198del	NM_001322256.1:c.193_198del	NM_001322256.1:c.194_198del	NM_001322256.1:c.195_198del	NM_001322256.1:c.196_198del	NM_001322256.1:c.197_198del	NM_001322256.1:c.*198del	NM_001322256.1:c.*198dup	NM_001322256.1:c.197_198dup	NM_001322256.1:c.196_198dup	NM_001322256.1:c.195_198dup	NM_001322256.1:c.192_198dup	NM_001322256.1:c.191_198dup	NM_001322256.1:c.190_198dup	NM_001322256.1:c.189_198dup	NM_001322256.1:c.188_198dup	NM_001322256.1:c.186_198dup	NM_001322256.1:c.177_198dup	NM_001322256.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 5	NM_001387866.1:c.175_198=	NM_001387866.1:c.185_198del	NM_001387866.1:c.186_198del	NM_001387866.1:c.187_198del	NM_001387866.1:c.188_198del	NM_001387866.1:c.189_198del	NM_001387866.1:c.191_198del	NM_001387866.1:c.192_198del	NM_001387866.1:c.193_198del	NM_001387866.1:c.194_198del	NM_001387866.1:c.195_198del	NM_001387866.1:c.196_198del	NM_001387866.1:c.197_198del	NM_001387866.1:c.*198del	NM_001387866.1:c.*198dup	NM_001387866.1:c.197_198dup	NM_001387866.1:c.196_198dup	NM_001387866.1:c.195_198dup	NM_001387866.1:c.192_198dup	NM_001387866.1:c.191_198dup	NM_001387866.1:c.190_198dup	NM_001387866.1:c.189_198dup	NM_001387866.1:c.188_198dup	NM_001387866.1:c.186_198dup	NM_001387866.1:c.177_198dup	NM_001387866.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 6	NM_001387867.1:c.175_198=	NM_001387867.1:c.185_198del	NM_001387867.1:c.186_198del	NM_001387867.1:c.187_198del	NM_001387867.1:c.188_198del	NM_001387867.1:c.189_198del	NM_001387867.1:c.191_198del	NM_001387867.1:c.192_198del	NM_001387867.1:c.193_198del	NM_001387867.1:c.194_198del	NM_001387867.1:c.195_198del	NM_001387867.1:c.196_198del	NM_001387867.1:c.197_198del	NM_001387867.1:c.*198del	NM_001387867.1:c.*198dup	NM_001387867.1:c.197_198dup	NM_001387867.1:c.196_198dup	NM_001387867.1:c.195_198dup	NM_001387867.1:c.192_198dup	NM_001387867.1:c.191_198dup	NM_001387867.1:c.190_198dup	NM_001387867.1:c.189_198dup	NM_001387867.1:c.188_198dup	NM_001387867.1:c.186_198dup	NM_001387867.1:c.177_198dup	NM_001387867.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 4	NM_001322257.1:c.175_198=	NM_001322257.1:c.185_198del	NM_001322257.1:c.186_198del	NM_001322257.1:c.187_198del	NM_001322257.1:c.188_198del	NM_001322257.1:c.189_198del	NM_001322257.1:c.191_198del	NM_001322257.1:c.192_198del	NM_001322257.1:c.193_198del	NM_001322257.1:c.194_198del	NM_001322257.1:c.195_198del	NM_001322257.1:c.196_198del	NM_001322257.1:c.197_198del	NM_001322257.1:c.*198del	NM_001322257.1:c.*198dup	NM_001322257.1:c.197_198dup	NM_001322257.1:c.196_198dup	NM_001322257.1:c.195_198dup	NM_001322257.1:c.192_198dup	NM_001322257.1:c.191_198dup	NM_001322257.1:c.190_198dup	NM_001322257.1:c.189_198dup	NM_001322257.1:c.188_198dup	NM_001322257.1:c.186_198dup	NM_001322257.1:c.177_198dup	NM_001322257.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 7	NM_001387869.1:c.175_198=	NM_001387869.1:c.185_198del	NM_001387869.1:c.186_198del	NM_001387869.1:c.187_198del	NM_001387869.1:c.188_198del	NM_001387869.1:c.189_198del	NM_001387869.1:c.191_198del	NM_001387869.1:c.192_198del	NM_001387869.1:c.193_198del	NM_001387869.1:c.194_198del	NM_001387869.1:c.195_198del	NM_001387869.1:c.196_198del	NM_001387869.1:c.197_198del	NM_001387869.1:c.*198del	NM_001387869.1:c.*198dup	NM_001387869.1:c.197_198dup	NM_001387869.1:c.196_198dup	NM_001387869.1:c.195_198dup	NM_001387869.1:c.192_198dup	NM_001387869.1:c.191_198dup	NM_001387869.1:c.190_198dup	NM_001387869.1:c.189_198dup	NM_001387869.1:c.188_198dup	NM_001387869.1:c.186_198dup	NM_001387869.1:c.177_198dup	NM_001387869.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

64 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41954375	Mar 13, 2006 (126)
2	HGSV	ss82150953	Dec 14, 2007 (130)
3	HGSV	ss82792969	Dec 14, 2007 (130)
4	HGSV	ss83384710	Dec 14, 2007 (130)
5	HUMANGENOME_JCVI	ss99166457	Feb 04, 2009 (130)
6	BCMHGSC_JDW	ss103668109	Mar 15, 2016 (147)
7	PJP	ss295100026	May 09, 2011 (134)
8	1000GENOMES	ss1370336764	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1703622619	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1703622764	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710080189	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710080267	Apr 01, 2015 (144)
13	SWEGEN	ss2992294649	Nov 08, 2017 (151)
14	URBANLAB	ss3647400876	Oct 12, 2018 (152)
15	EVA_DECODE	ss3709206042	Jul 13, 2019 (153)
16	EVA_DECODE	ss3709206043	Jul 13, 2019 (153)
17	EVA_DECODE	ss3709206044	Jul 13, 2019 (153)
18	EVA_DECODE	ss3709206045	Jul 13, 2019 (153)
19	PACBIO	ss3789827110	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3803154340	Jul 13, 2019 (153)
21	EVA	ss3827802636	Apr 25, 2020 (154)
22	GNOMAD	ss4070902450	Apr 26, 2021 (155)
23	GNOMAD	ss4070902451	Apr 26, 2021 (155)
24	GNOMAD	ss4070902452	Apr 26, 2021 (155)
25	GNOMAD	ss4070902453	Apr 26, 2021 (155)
26	GNOMAD	ss4070902454	Apr 26, 2021 (155)
27	GNOMAD	ss4070902455	Apr 26, 2021 (155)
28	GNOMAD	ss4070902456	Apr 26, 2021 (155)
29	GNOMAD	ss4070902457	Apr 26, 2021 (155)
30	GNOMAD	ss4070902458	Apr 26, 2021 (155)
31	GNOMAD	ss4070902459	Apr 26, 2021 (155)
32	GNOMAD	ss4070902460	Apr 26, 2021 (155)
33	GNOMAD	ss4070902461	Apr 26, 2021 (155)
34	GNOMAD	ss4070902462	Apr 26, 2021 (155)
35	GNOMAD	ss4070902463	Apr 26, 2021 (155)
36	GNOMAD	ss4070902464	Apr 26, 2021 (155)
37	GNOMAD	ss4070902465	Apr 26, 2021 (155)
38	GNOMAD	ss4070902466	Apr 26, 2021 (155)
39	GNOMAD	ss4070902467	Apr 26, 2021 (155)
40	GNOMAD	ss4070902468	Apr 26, 2021 (155)
41	GNOMAD	ss4070902469	Apr 26, 2021 (155)
42	GNOMAD	ss4070902470	Apr 26, 2021 (155)
43	GNOMAD	ss4070902471	Apr 26, 2021 (155)
44	GNOMAD	ss4070902472	Apr 26, 2021 (155)
45	GNOMAD	ss4070902473	Apr 26, 2021 (155)
46	GNOMAD	ss4070902474	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5159105877	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5159105878	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5159105879	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5159105880	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5159105881	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5254042472	Oct 12, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5254042474	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5254042475	Oct 12, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5254042476	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5453436860	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5453436861	Oct 12, 2022 (156)
58	SANFORD_IMAGENETICS	ss5632105391	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5690754603	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5690754604	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5690754606	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5690754607	Oct 12, 2022 (156)
63	EVA	ss5800106752	Oct 12, 2022 (156)
64	EVA	ss5980145770	Oct 12, 2022 (156)
65	1000Genomes	NC_000003.11 - 51697611	Oct 12, 2018 (152)
66	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 8417206 (NC_000003.11:51697611:A: 1953/3854) Row 8417207 (NC_000003.11:51697610:AAA: 1067/3854)	-	Oct 12, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 8417206 (NC_000003.11:51697611:A: 1953/3854) Row 8417207 (NC_000003.11:51697610:AAA: 1067/3854)	-	Oct 12, 2018 (152)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107455629 (NC_000003.12:51663594::A 253/41026) Row 107455630 (NC_000003.12:51663594::AA 8/41116) Row 107455631 (NC_000003.12:51663594::AAA 1/41120)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 17075184 (NC_000003.11:51697610:A: 6415/15890) Row 17075185 (NC_000003.11:51697610::A 142/15890) Row 17075186 (NC_000003.11:51697610:AA: 18/15890)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 17075184 (NC_000003.11:51697610:A: 6415/15890) Row 17075185 (NC_000003.11:51697610::A 142/15890) Row 17075186 (NC_000003.11:51697610:AA: 18/15890)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 17075184 (NC_000003.11:51697610:A: 6415/15890) Row 17075185 (NC_000003.11:51697610::A 142/15890) Row 17075186 (NC_000003.11:51697610:AA: 18/15890)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 17075184 (NC_000003.11:51697610:A: 6415/15890) Row 17075185 (NC_000003.11:51697610::A 142/15890) Row 17075186 (NC_000003.11:51697610:AA: 18/15890)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 17075184 (NC_000003.11:51697610:A: 6415/15890) Row 17075185 (NC_000003.11:51697610::A 142/15890) Row 17075186 (NC_000003.11:51697610:AA: 18/15890)...	-	Apr 26, 2021 (155)
98	14KJPN Submission ignored due to conflicting rows: Row 24591707 (NC_000003.12:51663594:A: 12120/26452) Row 24591708 (NC_000003.12:51663594::A 209/26452) Row 24591710 (NC_000003.12:51663594:AA: 27/26452)...	-	Oct 12, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 24591707 (NC_000003.12:51663594:A: 12120/26452) Row 24591708 (NC_000003.12:51663594::A 209/26452) Row 24591710 (NC_000003.12:51663594:AA: 27/26452)...	-	Oct 12, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 24591707 (NC_000003.12:51663594:A: 12120/26452) Row 24591708 (NC_000003.12:51663594::A 209/26452) Row 24591710 (NC_000003.12:51663594:AA: 27/26452)...	-	Oct 12, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 24591707 (NC_000003.12:51663594:A: 12120/26452) Row 24591708 (NC_000003.12:51663594::A 209/26452) Row 24591710 (NC_000003.12:51663594:AA: 27/26452)...	-	Oct 12, 2022 (156)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 8417206 (NC_000003.11:51697611:A: 1880/3708) Row 8417207 (NC_000003.11:51697610:AAA: 997/3708)	-	Oct 12, 2018 (152)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 8417206 (NC_000003.11:51697611:A: 1880/3708) Row 8417207 (NC_000003.11:51697610:AAA: 997/3708)	-	Oct 12, 2018 (152)
104	ALFA	NC_000003.12 - 51663595	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs57803391	May 24, 2008 (130)
rs77512922	Oct 12, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4070902474	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4070902473	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4070902472	NC_000003.12:51663594:AAAAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5159105881	NC_000003.11:51697610:AAAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4070902471, ss5254042475	NC_000003.12:51663594:AAAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4070902470	NC_000003.12:51663594:AAAAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4070902469	NC_000003.12:51663594:AAAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5159105880	NC_000003.11:51697610:AAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4070902468, ss5690754607	NC_000003.12:51663594:AAAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4070902467	NC_000003.12:51663594:AAAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4070902466	NC_000003.12:51663594:AAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss103668109	NT_022517.18:51637629:AAAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4070902465, ss5254042476	NC_000003.12:51663594:AAAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1703622619, ss1703622764, ss5800106752	NC_000003.11:51697610:AAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3709206045, ss4070902464	NC_000003.12:51663594:AAA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5159105879, ss5980145770	NC_000003.11:51697610:AA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710080189, ss1710080267	NC_000003.11:51697611:AA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902463, ss5254042474, ss5453436861, ss5690754606	NC_000003.12:51663594:AA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709206044	NC_000003.12:51663595:AA:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss82150953, ss82792969, ss83384710	NC_000003.9:51672673:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295100026	NC_000003.10:51672673:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
15136539, ss1370336764, ss2992294649, ss3789827110, ss3827802636, ss5159105877, ss5632105391	NC_000003.11:51697610:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000003.11:51697611:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3647400876, ss3803154340, ss4070902462, ss5453436860, ss5690754603	NC_000003.12:51663594:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709206043	NC_000003.12:51663596:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss41954375, ss99166457	NT_022517.18:51637633:A:	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159105878	NC_000003.11:51697610::A	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902450, ss5254042472, ss5690754604	NC_000003.12:51663594::A	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
3438098805	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709206042	NC_000003.12:51663597::A	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902451	NC_000003.12:51663594::AA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902452	NC_000003.12:51663594::AAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902453	NC_000003.12:51663594::AAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902454	NC_000003.12:51663594::AAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902455	NC_000003.12:51663594::AAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902456	NC_000003.12:51663594::AAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902457	NC_000003.12:51663594::AAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902458	NC_000003.12:51663594::AAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902459	NC_000003.12:51663594::AAAAAAAAAAA… NC_000003.12:51663594::AAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902460	NC_000003.12:51663594::AAAAAAAAAAA… NC_000003.12:51663594::AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4070902461	NC_000003.12:51663594::AAAAAAAAAAA… NC_000003.12:51663594::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:51663594:AAAAAAAAAAAA… NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34235841

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

Placement	(A)₂₄=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₃	dup(A)₂₂	ins(A)₂₅
GRCh38.p14 chr 3	NC_000003.12:g.51663595_51663618=	NC_000003.12:g.51663605_51663618del	NC_000003.12:g.51663606_51663618del	NC_000003.12:g.51663607_51663618del	NC_000003.12:g.51663608_51663618del	NC_000003.12:g.51663609_51663618del	NC_000003.12:g.51663611_51663618del	NC_000003.12:g.51663612_51663618del	NC_000003.12:g.51663613_51663618del	NC_000003.12:g.51663614_51663618del	NC_000003.12:g.51663615_51663618del	NC_000003.12:g.51663616_51663618del	NC_000003.12:g.51663617_51663618del	NC_000003.12:g.51663618del	NC_000003.12:g.51663618dup	NC_000003.12:g.51663617_51663618dup	NC_000003.12:g.51663616_51663618dup	NC_000003.12:g.51663615_51663618dup	NC_000003.12:g.51663612_51663618dup	NC_000003.12:g.51663611_51663618dup	NC_000003.12:g.51663610_51663618dup	NC_000003.12:g.51663609_51663618dup	NC_000003.12:g.51663608_51663618dup	NC_000003.12:g.51663606_51663618dup	NC_000003.12:g.51663597_51663618dup	NC_000003.12:g.51663618_51663619insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 3	NC_000003.11:g.51697611_51697634=	NC_000003.11:g.51697621_51697634del	NC_000003.11:g.51697622_51697634del	NC_000003.11:g.51697623_51697634del	NC_000003.11:g.51697624_51697634del	NC_000003.11:g.51697625_51697634del	NC_000003.11:g.51697627_51697634del	NC_000003.11:g.51697628_51697634del	NC_000003.11:g.51697629_51697634del	NC_000003.11:g.51697630_51697634del	NC_000003.11:g.51697631_51697634del	NC_000003.11:g.51697632_51697634del	NC_000003.11:g.51697633_51697634del	NC_000003.11:g.51697634del	NC_000003.11:g.51697634dup	NC_000003.11:g.51697633_51697634dup	NC_000003.11:g.51697632_51697634dup	NC_000003.11:g.51697631_51697634dup	NC_000003.11:g.51697628_51697634dup	NC_000003.11:g.51697627_51697634dup	NC_000003.11:g.51697626_51697634dup	NC_000003.11:g.51697625_51697634dup	NC_000003.11:g.51697624_51697634dup	NC_000003.11:g.51697622_51697634dup	NC_000003.11:g.51697613_51697634dup	NC_000003.11:g.51697634_51697635insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 2	NM_015106.4:c.175_198=	NM_015106.4:c.185_198del	NM_015106.4:c.186_198del	NM_015106.4:c.187_198del	NM_015106.4:c.188_198del	NM_015106.4:c.189_198del	NM_015106.4:c.191_198del	NM_015106.4:c.192_198del	NM_015106.4:c.193_198del	NM_015106.4:c.194_198del	NM_015106.4:c.195_198del	NM_015106.4:c.196_198del	NM_015106.4:c.197_198del	NM_015106.4:c.*198del	NM_015106.4:c.*198dup	NM_015106.4:c.197_198dup	NM_015106.4:c.196_198dup	NM_015106.4:c.195_198dup	NM_015106.4:c.192_198dup	NM_015106.4:c.191_198dup	NM_015106.4:c.190_198dup	NM_015106.4:c.189_198dup	NM_015106.4:c.188_198dup	NM_015106.4:c.186_198dup	NM_015106.4:c.177_198dup	NM_015106.4:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 2	NM_015106.3:c.175_198=	NM_015106.3:c.185_198del	NM_015106.3:c.186_198del	NM_015106.3:c.187_198del	NM_015106.3:c.188_198del	NM_015106.3:c.189_198del	NM_015106.3:c.191_198del	NM_015106.3:c.192_198del	NM_015106.3:c.193_198del	NM_015106.3:c.194_198del	NM_015106.3:c.195_198del	NM_015106.3:c.196_198del	NM_015106.3:c.197_198del	NM_015106.3:c.*198del	NM_015106.3:c.*198dup	NM_015106.3:c.197_198dup	NM_015106.3:c.196_198dup	NM_015106.3:c.195_198dup	NM_015106.3:c.192_198dup	NM_015106.3:c.191_198dup	NM_015106.3:c.190_198dup	NM_015106.3:c.189_198dup	NM_015106.3:c.188_198dup	NM_015106.3:c.186_198dup	NM_015106.3:c.177_198dup	NM_015106.3:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript	NM_015106.2:c.175_202=	NM_015106.2:c.189_202del	NM_015106.2:c.190_202del	NM_015106.2:c.191_202del	NM_015106.2:c.192_202del	NM_015106.2:c.193_202del	NM_015106.2:c.195_202del	NM_015106.2:c.196_202del	NM_015106.2:c.197_202del	NM_015106.2:c.198_202del	NM_015106.2:c.199_202del	NM_015106.2:c.200_202del	NM_015106.2:c.201_202del	NM_015106.2:c.*202del	NM_015106.2:c.*202dup	NM_015106.2:c.201_202dup	NM_015106.2:c.200_202dup	NM_015106.2:c.199_202dup	NM_015106.2:c.196_202dup	NM_015106.2:c.195_202dup	NM_015106.2:c.194_202dup	NM_015106.2:c.193_202dup	NM_015106.2:c.192_202dup	NM_015106.2:c.190_202dup	NM_015106.2:c.181_202dup	NM_015106.2:c.178_202dup
RAD54L2 transcript variant 1	NM_001322253.2:c.175_198=	NM_001322253.2:c.185_198del	NM_001322253.2:c.186_198del	NM_001322253.2:c.187_198del	NM_001322253.2:c.188_198del	NM_001322253.2:c.189_198del	NM_001322253.2:c.191_198del	NM_001322253.2:c.192_198del	NM_001322253.2:c.193_198del	NM_001322253.2:c.194_198del	NM_001322253.2:c.195_198del	NM_001322253.2:c.196_198del	NM_001322253.2:c.197_198del	NM_001322253.2:c.*198del	NM_001322253.2:c.*198dup	NM_001322253.2:c.197_198dup	NM_001322253.2:c.196_198dup	NM_001322253.2:c.195_198dup	NM_001322253.2:c.192_198dup	NM_001322253.2:c.191_198dup	NM_001322253.2:c.190_198dup	NM_001322253.2:c.189_198dup	NM_001322253.2:c.188_198dup	NM_001322253.2:c.186_198dup	NM_001322253.2:c.177_198dup	NM_001322253.2:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 1	NM_001322253.1:c.175_198=	NM_001322253.1:c.185_198del	NM_001322253.1:c.186_198del	NM_001322253.1:c.187_198del	NM_001322253.1:c.188_198del	NM_001322253.1:c.189_198del	NM_001322253.1:c.191_198del	NM_001322253.1:c.192_198del	NM_001322253.1:c.193_198del	NM_001322253.1:c.194_198del	NM_001322253.1:c.195_198del	NM_001322253.1:c.196_198del	NM_001322253.1:c.197_198del	NM_001322253.1:c.*198del	NM_001322253.1:c.*198dup	NM_001322253.1:c.197_198dup	NM_001322253.1:c.196_198dup	NM_001322253.1:c.195_198dup	NM_001322253.1:c.192_198dup	NM_001322253.1:c.191_198dup	NM_001322253.1:c.190_198dup	NM_001322253.1:c.189_198dup	NM_001322253.1:c.188_198dup	NM_001322253.1:c.186_198dup	NM_001322253.1:c.177_198dup	NM_001322253.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 3	NM_001322256.2:c.175_198=	NM_001322256.2:c.185_198del	NM_001322256.2:c.186_198del	NM_001322256.2:c.187_198del	NM_001322256.2:c.188_198del	NM_001322256.2:c.189_198del	NM_001322256.2:c.191_198del	NM_001322256.2:c.192_198del	NM_001322256.2:c.193_198del	NM_001322256.2:c.194_198del	NM_001322256.2:c.195_198del	NM_001322256.2:c.196_198del	NM_001322256.2:c.197_198del	NM_001322256.2:c.*198del	NM_001322256.2:c.*198dup	NM_001322256.2:c.197_198dup	NM_001322256.2:c.196_198dup	NM_001322256.2:c.195_198dup	NM_001322256.2:c.192_198dup	NM_001322256.2:c.191_198dup	NM_001322256.2:c.190_198dup	NM_001322256.2:c.189_198dup	NM_001322256.2:c.188_198dup	NM_001322256.2:c.186_198dup	NM_001322256.2:c.177_198dup	NM_001322256.2:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 3	NM_001322256.1:c.175_198=	NM_001322256.1:c.185_198del	NM_001322256.1:c.186_198del	NM_001322256.1:c.187_198del	NM_001322256.1:c.188_198del	NM_001322256.1:c.189_198del	NM_001322256.1:c.191_198del	NM_001322256.1:c.192_198del	NM_001322256.1:c.193_198del	NM_001322256.1:c.194_198del	NM_001322256.1:c.195_198del	NM_001322256.1:c.196_198del	NM_001322256.1:c.197_198del	NM_001322256.1:c.*198del	NM_001322256.1:c.*198dup	NM_001322256.1:c.197_198dup	NM_001322256.1:c.196_198dup	NM_001322256.1:c.195_198dup	NM_001322256.1:c.192_198dup	NM_001322256.1:c.191_198dup	NM_001322256.1:c.190_198dup	NM_001322256.1:c.189_198dup	NM_001322256.1:c.188_198dup	NM_001322256.1:c.186_198dup	NM_001322256.1:c.177_198dup	NM_001322256.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 5	NM_001387866.1:c.175_198=	NM_001387866.1:c.185_198del	NM_001387866.1:c.186_198del	NM_001387866.1:c.187_198del	NM_001387866.1:c.188_198del	NM_001387866.1:c.189_198del	NM_001387866.1:c.191_198del	NM_001387866.1:c.192_198del	NM_001387866.1:c.193_198del	NM_001387866.1:c.194_198del	NM_001387866.1:c.195_198del	NM_001387866.1:c.196_198del	NM_001387866.1:c.197_198del	NM_001387866.1:c.*198del	NM_001387866.1:c.*198dup	NM_001387866.1:c.197_198dup	NM_001387866.1:c.196_198dup	NM_001387866.1:c.195_198dup	NM_001387866.1:c.192_198dup	NM_001387866.1:c.191_198dup	NM_001387866.1:c.190_198dup	NM_001387866.1:c.189_198dup	NM_001387866.1:c.188_198dup	NM_001387866.1:c.186_198dup	NM_001387866.1:c.177_198dup	NM_001387866.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 6	NM_001387867.1:c.175_198=	NM_001387867.1:c.185_198del	NM_001387867.1:c.186_198del	NM_001387867.1:c.187_198del	NM_001387867.1:c.188_198del	NM_001387867.1:c.189_198del	NM_001387867.1:c.191_198del	NM_001387867.1:c.192_198del	NM_001387867.1:c.193_198del	NM_001387867.1:c.194_198del	NM_001387867.1:c.195_198del	NM_001387867.1:c.196_198del	NM_001387867.1:c.197_198del	NM_001387867.1:c.*198del	NM_001387867.1:c.*198dup	NM_001387867.1:c.197_198dup	NM_001387867.1:c.196_198dup	NM_001387867.1:c.195_198dup	NM_001387867.1:c.192_198dup	NM_001387867.1:c.191_198dup	NM_001387867.1:c.190_198dup	NM_001387867.1:c.189_198dup	NM_001387867.1:c.188_198dup	NM_001387867.1:c.186_198dup	NM_001387867.1:c.177_198dup	NM_001387867.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 4	NM_001322257.1:c.175_198=	NM_001322257.1:c.185_198del	NM_001322257.1:c.186_198del	NM_001322257.1:c.187_198del	NM_001322257.1:c.188_198del	NM_001322257.1:c.189_198del	NM_001322257.1:c.191_198del	NM_001322257.1:c.192_198del	NM_001322257.1:c.193_198del	NM_001322257.1:c.194_198del	NM_001322257.1:c.195_198del	NM_001322257.1:c.196_198del	NM_001322257.1:c.197_198del	NM_001322257.1:c.*198del	NM_001322257.1:c.*198dup	NM_001322257.1:c.197_198dup	NM_001322257.1:c.196_198dup	NM_001322257.1:c.195_198dup	NM_001322257.1:c.192_198dup	NM_001322257.1:c.191_198dup	NM_001322257.1:c.190_198dup	NM_001322257.1:c.189_198dup	NM_001322257.1:c.188_198dup	NM_001322257.1:c.186_198dup	NM_001322257.1:c.177_198dup	NM_001322257.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA
RAD54L2 transcript variant 7	NM_001387869.1:c.175_198=	NM_001387869.1:c.185_198del	NM_001387869.1:c.186_198del	NM_001387869.1:c.187_198del	NM_001387869.1:c.188_198del	NM_001387869.1:c.189_198del	NM_001387869.1:c.191_198del	NM_001387869.1:c.192_198del	NM_001387869.1:c.193_198del	NM_001387869.1:c.194_198del	NM_001387869.1:c.195_198del	NM_001387869.1:c.196_198del	NM_001387869.1:c.197_198del	NM_001387869.1:c.*198del	NM_001387869.1:c.*198dup	NM_001387869.1:c.197_198dup	NM_001387869.1:c.196_198dup	NM_001387869.1:c.195_198dup	NM_001387869.1:c.192_198dup	NM_001387869.1:c.191_198dup	NM_001387869.1:c.190_198dup	NM_001387869.1:c.189_198dup	NM_001387869.1:c.188_198dup	NM_001387869.1:c.186_198dup	NM_001387869.1:c.177_198dup	NM_001387869.1:c.198_199insAAAAAAAAAAAAAAAAAAAAAAAAA

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34235841