Name: rs34795556
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.

rs34795556

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:62082672-62082698 (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)₁₆ / del(A)₁₅ / del(A)₁₂ / d…
del(A)₁₆ / del(A)₁₅ / del(A)₁₂ / del(A)₁₁ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₆=0.4603 (2305/5008, 1000G)
del(A)₁₆=0.1674 (645/3854, ALSPAC)
del(A)₁₆=0.000 (0/130, ALFA) (+ 15 more)
del(A)₁₅=0.000 (0/130, ALFA)
del(A)₁₂=0.000 (0/130, ALFA)
del(A)₁₁=0.000 (0/130, ALFA)
del(A)₉=0.000 (0/130, ALFA)
del(A)₈=0.000 (0/130, ALFA)
del(A)₇=0.000 (0/130, ALFA)
del(A)₅=0.000 (0/130, ALFA)
del(A)₄=0.000 (0/130, ALFA)
delAAA=0.000 (0/130, ALFA)
delAA=0.000 (0/130, ALFA)
delA=0.000 (0/130, ALFA)
dupA=0.000 (0/130, ALFA)
dupAA=0.000 (0/130, ALFA)
dupAAA=0.000 (0/130, ALFA)
(A)₂₇=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADGRL3-AS1 : Intron 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	Alt HMOZ	HTRZ	HWEP
Total	Global	130	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	54	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	70	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	64	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₇=0.5397	del(A)₁₆=0.4603
1000Genomes	African	Sub	1322	(A)₂₇=0.4849	del(A)₁₆=0.5151
1000Genomes	East Asian	Sub	1008	(A)₂₇=0.5863	del(A)₁₆=0.4137
1000Genomes	Europe	Sub	1006	(A)₂₇=0.5050	del(A)₁₆=0.4950
1000Genomes	South Asian	Sub	978	(A)₂₇=0.559	del(A)₁₆=0.441
1000Genomes	American	Sub	694	(A)₂₇=0.599	del(A)₁₆=0.401
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₂₇=0.8326	del(A)₁₆=0.1674
Allele Frequency Aggregator	Total	Global	130	(A)₂₇=1.000	del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	70	(A)₂₇=1.00	del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	European	Sub	54	(A)₂₇=1.00	del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	4	(A)₂₇=1.0	del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(A)₂₇=1.0	del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₂₇=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₇=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₇=0	del(A)₁₆=0, del(A)₁₅=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₇=0.00	del(A)₁₆=1.00

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 4	NC_000004.12:g.62082683_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082684_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082687_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082688_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082690_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082691_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082692_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082694_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082695_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082696_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082697_62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082698del
GRCh38.p14 chr 4	NC_000004.12:g.62082698dup
GRCh38.p14 chr 4	NC_000004.12:g.62082697_62082698dup
GRCh38.p14 chr 4	NC_000004.12:g.62082696_62082698dup
GRCh37.p13 chr 4	NC_000004.11:g.62948401_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948402_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948405_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948406_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948408_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948409_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948410_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948412_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948413_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948414_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948415_62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948416del
GRCh37.p13 chr 4	NC_000004.11:g.62948416dup
GRCh37.p13 chr 4	NC_000004.11:g.62948415_62948416dup
GRCh37.p13 chr 4	NC_000004.11:g.62948414_62948416dup

Gene: ADGRL3-AS1, ADGRL3 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADGRL3-AS1 transcript	NR_110595.1:n.	N/A	Intron 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)₂₇=	del(A)₁₆	del(A)₁₅	del(A)₁₂	del(A)₁₁	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 4	NC_000004.12:g.62082672_62082698=	NC_000004.12:g.62082683_62082698del	NC_000004.12:g.62082684_62082698del	NC_000004.12:g.62082687_62082698del	NC_000004.12:g.62082688_62082698del	NC_000004.12:g.62082690_62082698del	NC_000004.12:g.62082691_62082698del	NC_000004.12:g.62082692_62082698del	NC_000004.12:g.62082694_62082698del	NC_000004.12:g.62082695_62082698del	NC_000004.12:g.62082696_62082698del	NC_000004.12:g.62082697_62082698del	NC_000004.12:g.62082698del	NC_000004.12:g.62082698dup	NC_000004.12:g.62082697_62082698dup	NC_000004.12:g.62082696_62082698dup
GRCh37.p13 chr 4	NC_000004.11:g.62948390_62948416=	NC_000004.11:g.62948401_62948416del	NC_000004.11:g.62948402_62948416del	NC_000004.11:g.62948405_62948416del	NC_000004.11:g.62948406_62948416del	NC_000004.11:g.62948408_62948416del	NC_000004.11:g.62948409_62948416del	NC_000004.11:g.62948410_62948416del	NC_000004.11:g.62948412_62948416del	NC_000004.11:g.62948413_62948416del	NC_000004.11:g.62948414_62948416del	NC_000004.11:g.62948415_62948416del	NC_000004.11:g.62948416del	NC_000004.11:g.62948416dup	NC_000004.11:g.62948415_62948416dup	NC_000004.11:g.62948414_62948416dup

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#.

52 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81856029	Dec 14, 2007 (142)
2	HUMANGENOME_JCVI	ss95356350	Mar 15, 2016 (147)
3	PJP	ss295167908	May 09, 2011 (138)
4	PJP	ss295167909	May 09, 2011 (134)
5	1000GENOMES	ss1372233271	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1578197902	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1704177895	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1704178691	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710149335	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710149337	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710149368	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710149370	Apr 01, 2015 (144)
13	SWEGEN	ss2994771688	Nov 08, 2017 (151)
14	URBANLAB	ss3647740577	Oct 12, 2018 (152)
15	EVA_DECODE	ss3712138195	Jul 13, 2019 (153)
16	EVA_DECODE	ss3712138196	Jul 13, 2019 (153)
17	EVA_DECODE	ss3712138197	Jul 13, 2019 (153)
18	EVA_DECODE	ss3712138198	Jul 13, 2019 (153)
19	EVA_DECODE	ss3712138199	Jul 13, 2019 (153)
20	EVA_DECODE	ss3712138200	Jul 13, 2019 (153)
21	PACBIO	ss3790181589	Jul 13, 2019 (153)
22	PACBIO	ss3790181590	Jul 13, 2019 (153)
23	PACBIO	ss3795056697	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3804988526	Jul 13, 2019 (153)
25	EVA	ss3828564113	Apr 26, 2020 (154)
26	GNOMAD	ss4112047752	Apr 26, 2021 (155)
27	GNOMAD	ss4112047753	Apr 26, 2021 (155)
28	GNOMAD	ss4112047754	Apr 26, 2021 (155)
29	GNOMAD	ss4112047755	Apr 26, 2021 (155)
30	GNOMAD	ss4112047756	Apr 26, 2021 (155)
31	GNOMAD	ss4112047757	Apr 26, 2021 (155)
32	GNOMAD	ss4112047758	Apr 26, 2021 (155)
33	GNOMAD	ss4112047759	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5165909938	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5165909939	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5165909940	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5165909941	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5165909942	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5259355802	Oct 17, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5259355803	Oct 17, 2022 (156)
41	HUGCELL_USP	ss5458097259	Oct 17, 2022 (156)
42	HUGCELL_USP	ss5458097260	Oct 17, 2022 (156)
43	HUGCELL_USP	ss5458097261	Oct 17, 2022 (156)
44	TOMMO_GENOMICS	ss5700308712	Oct 17, 2022 (156)
45	TOMMO_GENOMICS	ss5700308713	Oct 17, 2022 (156)
46	TOMMO_GENOMICS	ss5700308714	Oct 17, 2022 (156)
47	TOMMO_GENOMICS	ss5700308715	Oct 17, 2022 (156)
48	TOMMO_GENOMICS	ss5700308716	Oct 17, 2022 (156)
49	EVA	ss5844057197	Oct 17, 2022 (156)
50	EVA	ss5844057198	Oct 17, 2022 (156)
51	EVA	ss5844057199	Oct 17, 2022 (156)
52	EVA	ss5863614492	Oct 17, 2022 (156)
53	1000Genomes	NC_000004.11 - 62948390	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 62948390	Oct 12, 2018 (152)
55	The Danish reference pan genome	NC_000004.11 - 62948390	Apr 26, 2020 (154)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 151029289 (NC_000004.12:62082671::A 46/31034) Row 151029290 (NC_000004.12:62082671::AA 2/31034) Row 151029291 (NC_000004.12:62082671:AAAAA: 4/31034)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 23879245 (NC_000004.11:62948389:AA: 2977/16354) Row 23879246 (NC_000004.11:62948389:AAA: 3150/16354) Row 23879247 (NC_000004.11:62948389:A: 2674/16354)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 23879245 (NC_000004.11:62948389:AA: 2977/16354) Row 23879246 (NC_000004.11:62948389:AAA: 3150/16354) Row 23879247 (NC_000004.11:62948389:A: 2674/16354)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 23879245 (NC_000004.11:62948389:AA: 2977/16354) Row 23879246 (NC_000004.11:62948389:AAA: 3150/16354) Row 23879247 (NC_000004.11:62948389:A: 2674/16354)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 23879245 (NC_000004.11:62948389:AA: 2977/16354) Row 23879246 (NC_000004.11:62948389:AAA: 3150/16354) Row 23879247 (NC_000004.11:62948389:A: 2674/16354)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 23879245 (NC_000004.11:62948389:AA: 2977/16354) Row 23879246 (NC_000004.11:62948389:AAA: 3150/16354) Row 23879247 (NC_000004.11:62948389:A: 2674/16354)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 34145816 (NC_000004.12:62082671:AAA: 7389/27714) Row 34145817 (NC_000004.12:62082671:AA: 6895/27714) Row 34145818 (NC_000004.12:62082671:A: 5934/27714)...	-	Oct 17, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 34145816 (NC_000004.12:62082671:AAA: 7389/27714) Row 34145817 (NC_000004.12:62082671:AA: 6895/27714) Row 34145818 (NC_000004.12:62082671:A: 5934/27714)...	-	Oct 17, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 34145816 (NC_000004.12:62082671:AAA: 7389/27714) Row 34145817 (NC_000004.12:62082671:AA: 6895/27714) Row 34145818 (NC_000004.12:62082671:A: 5934/27714)...	-	Oct 17, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 34145816 (NC_000004.12:62082671:AAA: 7389/27714) Row 34145817 (NC_000004.12:62082671:AA: 6895/27714) Row 34145818 (NC_000004.12:62082671:A: 5934/27714)...	-	Oct 17, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 34145816 (NC_000004.12:62082671:AAA: 7389/27714) Row 34145817 (NC_000004.12:62082671:AA: 6895/27714) Row 34145818 (NC_000004.12:62082671:A: 5934/27714)...	-	Oct 17, 2022 (156)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11856316 (NC_000004.11:62948402:AAA: 1887/3708) Row 11856317 (NC_000004.11:62948403:AA: 929/3708) Row 11856318 (NC_000004.11:62948389:AAAAAAAAAAAAAAAA: 636/3708)	-	Apr 26, 2020 (154)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11856316 (NC_000004.11:62948402:AAA: 1887/3708) Row 11856317 (NC_000004.11:62948403:AA: 929/3708) Row 11856318 (NC_000004.11:62948389:AAAAAAAAAAAAAAAA: 636/3708)	-	Apr 26, 2020 (154)
76	UK 10K study - Twins	-	Oct 12, 2018 (152)
77	ALFA	NC_000004.12 - 62082672	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)
rs35285724	May 11, 2012 (137)
rs35912775	May 11, 2012 (137)
rs56696238	Aug 21, 2014 (142)
rs71213028	Oct 13, 2011 (136)
rs71932759	May 11, 2012 (137)
rs142648177	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
21312448, 11856318, 78987, ss1372233271, ss1578197902, ss1704177895, ss1704178691, ss2994771688, ss5844057198	NC_000004.11:62948389:AAAAAAAAAAAA… NC_000004.11:62948389:AAAAAAAAAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3712138200, ss3804988526, ss4112047759, ss5259355803, ss5458097259, ss5863614492	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4112047758	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4112047757	NC_000004.12:62082671:AAAAAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4112047756	NC_000004.12:62082671:AAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4112047755	NC_000004.12:62082671:AAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4112047754	NC_000004.12:62082671:AAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5165909941	NC_000004.11:62948389:AAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5259355802, ss5700308715	NC_000004.12:62082671:AAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712138199	NC_000004.12:62082683:AAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss81856029	NC_000004.9:62777179:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295167908	NC_000004.10:62631008:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5165909939, ss5844057197	NC_000004.11:62948389:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710149335, ss1710149368	NC_000004.11:62948402:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5458097260, ss5700308712	NC_000004.12:62082671:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712138198	NC_000004.12:62082684:AAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295167909	NC_000004.10:62631009:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3790181589, ss3795056697, ss5165909938, ss5844057199	NC_000004.11:62948389:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710149337, ss1710149370	NC_000004.11:62948403:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5458097261, ss5700308713	NC_000004.12:62082671:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712138197	NC_000004.12:62082685:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3647740577	NC_000004.12:62082695:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95356350	NT_022778.16:3159081:AA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3790181590, ss3828564113, ss5165909940	NC_000004.11:62948389:A:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5700308714	NC_000004.12:62082671:A:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712138196	NC_000004.12:62082686:A:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5165909942	NC_000004.11:62948389::A	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4112047752, ss5700308716	NC_000004.12:62082671::A	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3712138195	NC_000004.12:62082687::A	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4112047753	NC_000004.12:62082671::AA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4833914079	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3430216721	NC_000004.12:62082671::AAA	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ss3430216729	NC_000004.12:62082671:AAAAAAAAAAA:	NC_000004.12:62082671:AAAAAAAAAAAA… NC_000004.12:62082671:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

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

No publications for rs34795556

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

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34795556