Name: rs61284512
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.

rs61284512

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:46946462-46946479 (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)₇ / del(A)₆ / del(A)₅ / del(…
del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.3548 (1777/5008, 1000G)
del(A)₆=0.0000 (0/3370, ALFA)
del(A)₅=0.0000 (0/3370, ALFA) (+ 7 more)
del(A)₄=0.0000 (0/3370, ALFA)
delAAA=0.0000 (0/3370, ALFA)
delAA=0.0000 (0/3370, ALFA)
delA=0.0000 (0/3370, ALFA)
dupA=0.0000 (0/3370, ALFA)
dupAA=0.0000 (0/3370, ALFA)
dupAAA=0.0000 (0/3370, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GOSR2 : Intron Variant
LRRC37A2 : 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	HWEP
Total	Global	3370	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2036	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	930	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	32	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	898	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	32	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	22	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	32	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	160	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	22	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	158	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	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)₁₈=0.6452	delAA=0.3548
1000Genomes	African	Sub	1322	(A)₁₈=0.7980	delAA=0.2020
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.6091	delAA=0.3909
1000Genomes	Europe	Sub	1006	(A)₁₈=0.5636	delAA=0.4364
1000Genomes	South Asian	Sub	978	(A)₁₈=0.530	delAA=0.470
1000Genomes	American	Sub	694	(A)₁₈=0.687	delAA=0.313
Allele Frequency Aggregator	Total	Global	3370	(A)₁₈=1.0000	del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	2036	(A)₁₈=1.0000	del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	930	(A)₁₈=1.000	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, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	160	(A)₁₈=1.000	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, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	158	(A)₁₈=1.000	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, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	32	(A)₁₈=1.00	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, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	32	(A)₁₈=1.00	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, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(A)₁₈=1.00	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, dupAA=0.00, dupAAA=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 17	NC_000017.11:g.46946473_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946474_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946475_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946476_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946477_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946478_46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946479del
GRCh38.p14 chr 17	NC_000017.11:g.46946479dup
GRCh38.p14 chr 17	NC_000017.11:g.46946478_46946479dup
GRCh38.p14 chr 17	NC_000017.11:g.46946477_46946479dup
GRCh37.p13 chr 17	NC_000017.10:g.45023839_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023840_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023841_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023842_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023843_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023844_45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023845del
GRCh37.p13 chr 17	NC_000017.10:g.45023845dup
GRCh37.p13 chr 17	NC_000017.10:g.45023844_45023845dup
GRCh37.p13 chr 17	NC_000017.10:g.45023843_45023845dup
GOSR2 RefSeqGene	NG_031806.2:g.28354_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28355_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28356_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28357_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28358_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28359_28360del
GOSR2 RefSeqGene	NG_031806.2:g.28360del
GOSR2 RefSeqGene	NG_031806.2:g.28360dup
GOSR2 RefSeqGene	NG_031806.2:g.28359_28360dup
GOSR2 RefSeqGene	NG_031806.2:g.28358_28360dup

Gene: GOSR2, golgi SNAP receptor complex member 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GOSR2 transcript variant D	NM_001321133.2:c.583+7769… NM_001321133.2:c.583+7769_583+7775del	N/A	Intron Variant
GOSR2 transcript variant C	NM_001012511.3:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant E	NM_001321134.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant F	NM_001330252.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant G	NM_001353114.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant H	NM_001353115.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant I	NM_001353116.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant M	NM_001363851.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant A	NM_004287.5:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant B	NM_054022.4:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant J	NR_148349.2:n.	N/A	Intron Variant
GOSR2 transcript variant K	NR_148350.2:n.	N/A	Intron Variant
GOSR2 transcript variant L	NR_148351.2:n.	N/A	Intron Variant
GOSR2 transcript variant X4	XM_006722190.5:c.583+7769… XM_006722190.5:c.583+7769_583+7775del	N/A	Intron Variant
GOSR2 transcript variant X8	XM_011525501.4:c.584-2470… XM_011525501.4:c.584-2470_584-2464del	N/A	Intron Variant
GOSR2 transcript variant X9	XM_011525502.4:c.584-6190… XM_011525502.4:c.584-6190_584-6184del	N/A	Intron Variant
GOSR2 transcript variant X1	XM_017025378.2:c.580+7769… XM_017025378.2:c.580+7769_580+7775del	N/A	Intron Variant
GOSR2 transcript variant X3	XM_017025383.3:c.583+7769… XM_017025383.3:c.583+7769_583+7775del	N/A	Intron Variant
GOSR2 transcript variant X5	XM_017025386.2:c.442+7769… XM_017025386.2:c.442+7769_442+7775del	N/A	Intron Variant
GOSR2 transcript variant X6	XM_017025387.2:c.439+7769… XM_017025387.2:c.439+7769_439+7775del	N/A	Intron Variant
GOSR2 transcript variant X21	XM_017025389.2:c.530-901_… XM_017025389.2:c.530-901_530-895del	N/A	Intron Variant
GOSR2 transcript variant X10	XM_017025392.2:c.442+7769… XM_017025392.2:c.442+7769_442+7775del	N/A	Intron Variant
GOSR2 transcript variant X12	XM_047437112.1:c.584-901_… XM_047437112.1:c.584-901_584-895del	N/A	Intron Variant
GOSR2 transcript variant X15	XM_047437113.1:c.581-901_… XM_047437113.1:c.581-901_581-895del	N/A	Intron Variant
GOSR2 transcript variant X16	XM_047437114.1:c.530-901_… XM_047437114.1:c.530-901_530-895del	N/A	Intron Variant
GOSR2 transcript variant X17	XM_047437115.1:c.527-901_… XM_047437115.1:c.527-901_527-895del	N/A	Intron Variant
GOSR2 transcript variant X2	XM_047437116.1:c.583+7769… XM_047437116.1:c.583+7769_583+7775del	N/A	Intron Variant
GOSR2 transcript variant X18	XM_047437117.1:c.443-901_… XM_047437117.1:c.443-901_443-895del	N/A	Intron Variant
GOSR2 transcript variant X19	XM_047437118.1:c.440-901_… XM_047437118.1:c.440-901_440-895del	N/A	Intron Variant
GOSR2 transcript variant X7	XM_047437119.1:c.583+7769… XM_047437119.1:c.583+7769_583+7775del	N/A	Intron Variant
GOSR2 transcript variant X11	XM_047437120.1:c.442+7769… XM_047437120.1:c.442+7769_442+7775del	N/A	Intron Variant
GOSR2 transcript variant X13	XR_007065552.1:n.	N/A	Intron Variant
GOSR2 transcript variant X14	XR_007065553.1:n.	N/A	Intron Variant
GOSR2 transcript variant X20	XR_934616.4:n.	N/A	Intron Variant

Gene: LRRC37A2, leucine rich repeat containing 37 member A2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LRRC37A2 transcript variant 1	NM_001006607.3:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant 2	NM_001385803.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X16	XM_024450773.2:c.4810-102… XM_024450773.2:c.4810-102583_4810-102577del	N/A	Intron Variant
LRRC37A2 transcript variant X1	XM_011524841.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X2	XM_011524842.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X3	XM_011524843.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X4	XM_011524844.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X5	XM_011524846.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X7	XM_011524848.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X9	XM_011524849.3:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X10	XM_011524850.4:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X14	XM_047436141.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X15	XM_047436142.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X6	XM_047436143.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X8	XM_047436144.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X11	XM_047436145.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X17	XM_047436146.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X12	XM_047436147.1:c.	N/A	Genic Downstream Transcript Variant
LRRC37A2 transcript variant X13	XR_007065300.1:n.	N/A	Genic Downstream Transcript 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)₁₈=	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 17	NC_000017.11:g.46946462_46946479=	NC_000017.11:g.46946473_46946479del	NC_000017.11:g.46946474_46946479del	NC_000017.11:g.46946475_46946479del	NC_000017.11:g.46946476_46946479del	NC_000017.11:g.46946477_46946479del	NC_000017.11:g.46946478_46946479del	NC_000017.11:g.46946479del	NC_000017.11:g.46946479dup	NC_000017.11:g.46946478_46946479dup	NC_000017.11:g.46946477_46946479dup
GRCh37.p13 chr 17	NC_000017.10:g.45023828_45023845=	NC_000017.10:g.45023839_45023845del	NC_000017.10:g.45023840_45023845del	NC_000017.10:g.45023841_45023845del	NC_000017.10:g.45023842_45023845del	NC_000017.10:g.45023843_45023845del	NC_000017.10:g.45023844_45023845del	NC_000017.10:g.45023845del	NC_000017.10:g.45023845dup	NC_000017.10:g.45023844_45023845dup	NC_000017.10:g.45023843_45023845dup
GOSR2 RefSeqGene	NG_031806.2:g.28343_28360=	NG_031806.2:g.28354_28360del	NG_031806.2:g.28355_28360del	NG_031806.2:g.28356_28360del	NG_031806.2:g.28357_28360del	NG_031806.2:g.28358_28360del	NG_031806.2:g.28359_28360del	NG_031806.2:g.28360del	NG_031806.2:g.28360dup	NG_031806.2:g.28359_28360dup	NG_031806.2:g.28358_28360dup
GOSR2 transcript variant D	NM_001321133.2:c.583+7758=	NM_001321133.2:c.583+7769_583+7775del	NM_001321133.2:c.583+7770_583+7775del	NM_001321133.2:c.583+7771_583+7775del	NM_001321133.2:c.583+7772_583+7775del	NM_001321133.2:c.583+7773_583+7775del	NM_001321133.2:c.583+7774_583+7775del	NM_001321133.2:c.583+7775del	NM_001321133.2:c.583+7775dup	NM_001321133.2:c.583+7774_583+7775dup	NM_001321133.2:c.583+7773_583+7775dup
GOSR2 transcript variant X1	XM_005257843.1:c.583+7758=	XM_005257843.1:c.583+7769_583+7775del	XM_005257843.1:c.583+7770_583+7775del	XM_005257843.1:c.583+7771_583+7775del	XM_005257843.1:c.583+7772_583+7775del	XM_005257843.1:c.583+7773_583+7775del	XM_005257843.1:c.583+7774_583+7775del	XM_005257843.1:c.583+7775del	XM_005257843.1:c.583+7775dup	XM_005257843.1:c.583+7774_583+7775dup	XM_005257843.1:c.583+7773_583+7775dup
GOSR2 transcript variant X4	XM_006722190.5:c.583+7758=	XM_006722190.5:c.583+7769_583+7775del	XM_006722190.5:c.583+7770_583+7775del	XM_006722190.5:c.583+7771_583+7775del	XM_006722190.5:c.583+7772_583+7775del	XM_006722190.5:c.583+7773_583+7775del	XM_006722190.5:c.583+7774_583+7775del	XM_006722190.5:c.583+7775del	XM_006722190.5:c.583+7775dup	XM_006722190.5:c.583+7774_583+7775dup	XM_006722190.5:c.583+7773_583+7775dup
GOSR2 transcript variant X8	XM_011525501.4:c.584-2481=	XM_011525501.4:c.584-2470_584-2464del	XM_011525501.4:c.584-2469_584-2464del	XM_011525501.4:c.584-2468_584-2464del	XM_011525501.4:c.584-2467_584-2464del	XM_011525501.4:c.584-2466_584-2464del	XM_011525501.4:c.584-2465_584-2464del	XM_011525501.4:c.584-2464del	XM_011525501.4:c.584-2464dup	XM_011525501.4:c.584-2465_584-2464dup	XM_011525501.4:c.584-2466_584-2464dup
GOSR2 transcript variant X9	XM_011525502.4:c.584-6201=	XM_011525502.4:c.584-6190_584-6184del	XM_011525502.4:c.584-6189_584-6184del	XM_011525502.4:c.584-6188_584-6184del	XM_011525502.4:c.584-6187_584-6184del	XM_011525502.4:c.584-6186_584-6184del	XM_011525502.4:c.584-6185_584-6184del	XM_011525502.4:c.584-6184del	XM_011525502.4:c.584-6184dup	XM_011525502.4:c.584-6185_584-6184dup	XM_011525502.4:c.584-6186_584-6184dup
GOSR2 transcript variant X1	XM_017025378.2:c.580+7758=	XM_017025378.2:c.580+7769_580+7775del	XM_017025378.2:c.580+7770_580+7775del	XM_017025378.2:c.580+7771_580+7775del	XM_017025378.2:c.580+7772_580+7775del	XM_017025378.2:c.580+7773_580+7775del	XM_017025378.2:c.580+7774_580+7775del	XM_017025378.2:c.580+7775del	XM_017025378.2:c.580+7775dup	XM_017025378.2:c.580+7774_580+7775dup	XM_017025378.2:c.580+7773_580+7775dup
GOSR2 transcript variant X3	XM_017025383.3:c.583+7758=	XM_017025383.3:c.583+7769_583+7775del	XM_017025383.3:c.583+7770_583+7775del	XM_017025383.3:c.583+7771_583+7775del	XM_017025383.3:c.583+7772_583+7775del	XM_017025383.3:c.583+7773_583+7775del	XM_017025383.3:c.583+7774_583+7775del	XM_017025383.3:c.583+7775del	XM_017025383.3:c.583+7775dup	XM_017025383.3:c.583+7774_583+7775dup	XM_017025383.3:c.583+7773_583+7775dup
GOSR2 transcript variant X5	XM_017025386.2:c.442+7758=	XM_017025386.2:c.442+7769_442+7775del	XM_017025386.2:c.442+7770_442+7775del	XM_017025386.2:c.442+7771_442+7775del	XM_017025386.2:c.442+7772_442+7775del	XM_017025386.2:c.442+7773_442+7775del	XM_017025386.2:c.442+7774_442+7775del	XM_017025386.2:c.442+7775del	XM_017025386.2:c.442+7775dup	XM_017025386.2:c.442+7774_442+7775dup	XM_017025386.2:c.442+7773_442+7775dup
GOSR2 transcript variant X6	XM_017025387.2:c.439+7758=	XM_017025387.2:c.439+7769_439+7775del	XM_017025387.2:c.439+7770_439+7775del	XM_017025387.2:c.439+7771_439+7775del	XM_017025387.2:c.439+7772_439+7775del	XM_017025387.2:c.439+7773_439+7775del	XM_017025387.2:c.439+7774_439+7775del	XM_017025387.2:c.439+7775del	XM_017025387.2:c.439+7775dup	XM_017025387.2:c.439+7774_439+7775dup	XM_017025387.2:c.439+7773_439+7775dup
GOSR2 transcript variant X21	XM_017025389.2:c.530-912=	XM_017025389.2:c.530-901_530-895del	XM_017025389.2:c.530-900_530-895del	XM_017025389.2:c.530-899_530-895del	XM_017025389.2:c.530-898_530-895del	XM_017025389.2:c.530-897_530-895del	XM_017025389.2:c.530-896_530-895del	XM_017025389.2:c.530-895del	XM_017025389.2:c.530-895dup	XM_017025389.2:c.530-896_530-895dup	XM_017025389.2:c.530-897_530-895dup
GOSR2 transcript variant X10	XM_017025392.2:c.442+7758=	XM_017025392.2:c.442+7769_442+7775del	XM_017025392.2:c.442+7770_442+7775del	XM_017025392.2:c.442+7771_442+7775del	XM_017025392.2:c.442+7772_442+7775del	XM_017025392.2:c.442+7773_442+7775del	XM_017025392.2:c.442+7774_442+7775del	XM_017025392.2:c.442+7775del	XM_017025392.2:c.442+7775dup	XM_017025392.2:c.442+7774_442+7775dup	XM_017025392.2:c.442+7773_442+7775dup
LRRC37A2 transcript variant X16	XM_024450773.2:c.4810-102594=	XM_024450773.2:c.4810-102583_4810-102577del	XM_024450773.2:c.4810-102582_4810-102577del	XM_024450773.2:c.4810-102581_4810-102577del	XM_024450773.2:c.4810-102580_4810-102577del	XM_024450773.2:c.4810-102579_4810-102577del	XM_024450773.2:c.4810-102578_4810-102577del	XM_024450773.2:c.4810-102577del	XM_024450773.2:c.4810-102577dup	XM_024450773.2:c.4810-102578_4810-102577dup	XM_024450773.2:c.4810-102579_4810-102577dup
GOSR2 transcript variant X12	XM_047437112.1:c.584-912=	XM_047437112.1:c.584-901_584-895del	XM_047437112.1:c.584-900_584-895del	XM_047437112.1:c.584-899_584-895del	XM_047437112.1:c.584-898_584-895del	XM_047437112.1:c.584-897_584-895del	XM_047437112.1:c.584-896_584-895del	XM_047437112.1:c.584-895del	XM_047437112.1:c.584-895dup	XM_047437112.1:c.584-896_584-895dup	XM_047437112.1:c.584-897_584-895dup
GOSR2 transcript variant X15	XM_047437113.1:c.581-912=	XM_047437113.1:c.581-901_581-895del	XM_047437113.1:c.581-900_581-895del	XM_047437113.1:c.581-899_581-895del	XM_047437113.1:c.581-898_581-895del	XM_047437113.1:c.581-897_581-895del	XM_047437113.1:c.581-896_581-895del	XM_047437113.1:c.581-895del	XM_047437113.1:c.581-895dup	XM_047437113.1:c.581-896_581-895dup	XM_047437113.1:c.581-897_581-895dup
GOSR2 transcript variant X16	XM_047437114.1:c.530-912=	XM_047437114.1:c.530-901_530-895del	XM_047437114.1:c.530-900_530-895del	XM_047437114.1:c.530-899_530-895del	XM_047437114.1:c.530-898_530-895del	XM_047437114.1:c.530-897_530-895del	XM_047437114.1:c.530-896_530-895del	XM_047437114.1:c.530-895del	XM_047437114.1:c.530-895dup	XM_047437114.1:c.530-896_530-895dup	XM_047437114.1:c.530-897_530-895dup
GOSR2 transcript variant X17	XM_047437115.1:c.527-912=	XM_047437115.1:c.527-901_527-895del	XM_047437115.1:c.527-900_527-895del	XM_047437115.1:c.527-899_527-895del	XM_047437115.1:c.527-898_527-895del	XM_047437115.1:c.527-897_527-895del	XM_047437115.1:c.527-896_527-895del	XM_047437115.1:c.527-895del	XM_047437115.1:c.527-895dup	XM_047437115.1:c.527-896_527-895dup	XM_047437115.1:c.527-897_527-895dup
GOSR2 transcript variant X2	XM_047437116.1:c.583+7758=	XM_047437116.1:c.583+7769_583+7775del	XM_047437116.1:c.583+7770_583+7775del	XM_047437116.1:c.583+7771_583+7775del	XM_047437116.1:c.583+7772_583+7775del	XM_047437116.1:c.583+7773_583+7775del	XM_047437116.1:c.583+7774_583+7775del	XM_047437116.1:c.583+7775del	XM_047437116.1:c.583+7775dup	XM_047437116.1:c.583+7774_583+7775dup	XM_047437116.1:c.583+7773_583+7775dup
GOSR2 transcript variant X18	XM_047437117.1:c.443-912=	XM_047437117.1:c.443-901_443-895del	XM_047437117.1:c.443-900_443-895del	XM_047437117.1:c.443-899_443-895del	XM_047437117.1:c.443-898_443-895del	XM_047437117.1:c.443-897_443-895del	XM_047437117.1:c.443-896_443-895del	XM_047437117.1:c.443-895del	XM_047437117.1:c.443-895dup	XM_047437117.1:c.443-896_443-895dup	XM_047437117.1:c.443-897_443-895dup
GOSR2 transcript variant X19	XM_047437118.1:c.440-912=	XM_047437118.1:c.440-901_440-895del	XM_047437118.1:c.440-900_440-895del	XM_047437118.1:c.440-899_440-895del	XM_047437118.1:c.440-898_440-895del	XM_047437118.1:c.440-897_440-895del	XM_047437118.1:c.440-896_440-895del	XM_047437118.1:c.440-895del	XM_047437118.1:c.440-895dup	XM_047437118.1:c.440-896_440-895dup	XM_047437118.1:c.440-897_440-895dup
GOSR2 transcript variant X7	XM_047437119.1:c.583+7758=	XM_047437119.1:c.583+7769_583+7775del	XM_047437119.1:c.583+7770_583+7775del	XM_047437119.1:c.583+7771_583+7775del	XM_047437119.1:c.583+7772_583+7775del	XM_047437119.1:c.583+7773_583+7775del	XM_047437119.1:c.583+7774_583+7775del	XM_047437119.1:c.583+7775del	XM_047437119.1:c.583+7775dup	XM_047437119.1:c.583+7774_583+7775dup	XM_047437119.1:c.583+7773_583+7775dup
GOSR2 transcript variant X11	XM_047437120.1:c.442+7758=	XM_047437120.1:c.442+7769_442+7775del	XM_047437120.1:c.442+7770_442+7775del	XM_047437120.1:c.442+7771_442+7775del	XM_047437120.1:c.442+7772_442+7775del	XM_047437120.1:c.442+7773_442+7775del	XM_047437120.1:c.442+7774_442+7775del	XM_047437120.1:c.442+7775del	XM_047437120.1:c.442+7775dup	XM_047437120.1:c.442+7774_442+7775dup	XM_047437120.1:c.442+7773_442+7775dup

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#.

48 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81592180	Dec 16, 2007 (129)
2	HUMANGENOME_JCVI	ss95694963	Dec 05, 2013 (138)
3	HUMANGENOME_JCVI	ss96568316	Dec 05, 2013 (138)
4	BILGI_BIOE	ss666692585	Apr 25, 2013 (138)
5	1000GENOMES	ss1376680460	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1708769786	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1708769834	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710732772	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710732775	Apr 01, 2015 (144)
10	MCHAISSO	ss3064712507	Nov 08, 2017 (151)
11	EVA_DECODE	ss3700524151	Jul 13, 2019 (153)
12	EVA_DECODE	ss3700524152	Jul 13, 2019 (153)
13	EVA_DECODE	ss3700524153	Jul 13, 2019 (153)
14	EVA_DECODE	ss3700524154	Jul 13, 2019 (153)
15	PACBIO	ss3788215267	Jul 13, 2019 (153)
16	PACBIO	ss3788215268	Jul 13, 2019 (153)
17	PACBIO	ss3793170918	Jul 13, 2019 (153)
18	PACBIO	ss3798056684	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3819968153	Jul 13, 2019 (153)
20	EVA	ss3834882435	Apr 27, 2020 (154)
21	GNOMAD	ss4312131385	Apr 27, 2021 (155)
22	GNOMAD	ss4312131386	Apr 27, 2021 (155)
23	GNOMAD	ss4312131387	Apr 27, 2021 (155)
24	GNOMAD	ss4312131388	Apr 27, 2021 (155)
25	GNOMAD	ss4312131389	Apr 27, 2021 (155)
26	GNOMAD	ss4312131390	Apr 27, 2021 (155)
27	GNOMAD	ss4312131391	Apr 27, 2021 (155)
28	GNOMAD	ss4312131392	Apr 27, 2021 (155)
29	GNOMAD	ss4312131393	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5222563464	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5222563465	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5222563466	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5222563467	Apr 27, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5303236388	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5303236389	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5303236391	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5303236392	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5496275267	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5496275268	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5496275269	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5496275271	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5778821442	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5778821443	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5778821444	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5778821445	Oct 16, 2022 (156)
46	EVA	ss5834024315	Oct 16, 2022 (156)
47	EVA	ss5834024316	Oct 16, 2022 (156)
48	EVA	ss5980969750	Oct 16, 2022 (156)
49	1000Genomes	NC_000017.10 - 45023828	Oct 12, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39906007 (NC_000017.10:45023828:A: 2130/3854) Row 39906008 (NC_000017.10:45023827:AAA: 219/3854)	-	Oct 12, 2018 (152)
51	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39906007 (NC_000017.10:45023828:A: 2130/3854) Row 39906008 (NC_000017.10:45023827:AAA: 219/3854)	-	Oct 12, 2018 (152)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508106619 (NC_000017.11:46946461::A 1902/90456) Row 508106620 (NC_000017.11:46946461::AA 19/90544) Row 508106621 (NC_000017.11:46946461::AAA 7/90548)...	-	Apr 27, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 80532771 (NC_000017.10:45023827:AA: 6552/16534) Row 80532772 (NC_000017.10:45023827:A: 741/16534) Row 80532773 (NC_000017.10:45023827::A 91/16534)...	-	Apr 27, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 80532771 (NC_000017.10:45023827:AA: 6552/16534) Row 80532772 (NC_000017.10:45023827:A: 741/16534) Row 80532773 (NC_000017.10:45023827::A 91/16534)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 80532771 (NC_000017.10:45023827:AA: 6552/16534) Row 80532772 (NC_000017.10:45023827:A: 741/16534) Row 80532773 (NC_000017.10:45023827::A 91/16534)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 80532771 (NC_000017.10:45023827:AA: 6552/16534) Row 80532772 (NC_000017.10:45023827:A: 741/16534) Row 80532773 (NC_000017.10:45023827::A 91/16534)...	-	Apr 27, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 112658546 (NC_000017.11:46946461:AA: 11893/28054) Row 112658547 (NC_000017.11:46946461:A: 1326/28054) Row 112658548 (NC_000017.11:46946461::A 138/28054)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 112658546 (NC_000017.11:46946461:AA: 11893/28054) Row 112658547 (NC_000017.11:46946461:A: 1326/28054) Row 112658548 (NC_000017.11:46946461::A 138/28054)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 112658546 (NC_000017.11:46946461:AA: 11893/28054) Row 112658547 (NC_000017.11:46946461:A: 1326/28054) Row 112658548 (NC_000017.11:46946461::A 138/28054)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 112658546 (NC_000017.11:46946461:AA: 11893/28054) Row 112658547 (NC_000017.11:46946461:A: 1326/28054) Row 112658548 (NC_000017.11:46946461::A 138/28054)...	-	Oct 16, 2022 (156)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39906007 (NC_000017.10:45023828:A: 2035/3708) Row 39906008 (NC_000017.10:45023827:AAA: 186/3708)	-	Oct 12, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39906007 (NC_000017.10:45023828:A: 2035/3708) Row 39906008 (NC_000017.10:45023827:AAA: 186/3708)	-	Oct 12, 2018 (152)
71	ALFA	NC_000017.11 - 46946462	Apr 27, 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)
rs71365018	May 11, 2012 (137)
rs71138562	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4312131393	NC_000017.11:46946461:AAAAAAA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4312131392	NC_000017.11:46946461:AAAAA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4312131391	NC_000017.11:46946461:AAAA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1708769786, ss1708769834, ss3788215267, ss5222563467, ss5834024316	NC_000017.10:45023827:AAA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3700524154, ss4312131390, ss5496275268, ss5778821445	NC_000017.11:46946461:AAA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss81592180	NC_000017.9:42378842:AA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
72011468, ss666692585, ss1376680460, ss3788215268, ss3793170918, ss3798056684, ss5222563464, ss5834024315, ss5980969750	NC_000017.10:45023827:AA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1710732772, ss1710732775	NC_000017.10:45023828:AA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3064712507, ss3819968153, ss4312131389, ss5303236388, ss5496275269, ss5778821442	NC_000017.11:46946461:AA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3700524153	NC_000017.11:46946462:AA:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3834882435, ss5222563465	NC_000017.10:45023827:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
	NC_000017.10:45023828:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4312131388, ss5303236389, ss5496275267, ss5778821443	NC_000017.11:46946461:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3700524152	NC_000017.11:46946463:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss96568316	NT_010783.15:10297979:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95694963	NT_010783.15:10297996:A:	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5222563466	NC_000017.10:45023827::A	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4312131385, ss5303236391, ss5496275271, ss5778821444	NC_000017.11:46946461::A	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3700524151	NC_000017.11:46946464::A	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4312131386, ss5303236392	NC_000017.11:46946461::AA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4312131387	NC_000017.11:46946461::AAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12270390822	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000017.11:46946461:AAAAAAAAAAAA… NC_000017.11:46946461:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs61284512

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

rs61284512