Name: rs60617461
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.

rs60617461

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:31136837-31136873 (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(AATG)₅ / del(AATG)₄ / del(AATG…
del(AATG)₅ / del(AATG)₄ / del(AATG)₃ / del(AATG)₂ / delAATG / dupAATG / dup(AATG)₂ / dup(AATG)₃ / dup(AATG)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupAATG=0.1690 (1267/7496, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: WRN : 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	7496	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.6988	GAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.1306, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.1690, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0016, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0000	0.749015	0.061583	0.189402	32
European	Sub	6291	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.6414	GAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.1555, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.2012, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0019, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0000	0.680201	0.078467	0.241332	32
African	Sub	766	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.000	GAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.00	GAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00	1.0	0.0	0.0	N/A
African American	Sub	734	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.000	GAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000	1.0	0.0	0.0	N/A
Asian	Sub	50	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.00	GAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.00	GAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.0	GAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	48	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.00	GAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	198	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.000	GAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	18	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=1.00	GAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.00	1.0	0.0	0.0	N/A
Other	Sub	125	GAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.984	GAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATG=0.008, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.008, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000, GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG=0.000	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7496	(GAAT)₉G=0.6988	del(AATG)₅=0.0000, del(AATG)₄=0.0000, del(AATG)₃=0.0000, del(AATG)₂=0.0000, delAATG=0.1306, dupAATG=0.1690, dup(AATG)₂=0.0016, dup(AATG)₃=0.0000, dup(AATG)₄=0.0000
Allele Frequency Aggregator	European	Sub	6291	(GAAT)₉G=0.6414	del(AATG)₅=0.0000, del(AATG)₄=0.0000, del(AATG)₃=0.0000, del(AATG)₂=0.0000, delAATG=0.1555, dupAATG=0.2012, dup(AATG)₂=0.0019, dup(AATG)₃=0.0000, dup(AATG)₄=0.0000
Allele Frequency Aggregator	African	Sub	766	(GAAT)₉G=1.000	del(AATG)₅=0.000, del(AATG)₄=0.000, del(AATG)₃=0.000, del(AATG)₂=0.000, delAATG=0.000, dupAATG=0.000, dup(AATG)₂=0.000, dup(AATG)₃=0.000, dup(AATG)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	198	(GAAT)₉G=1.000	del(AATG)₅=0.000, del(AATG)₄=0.000, del(AATG)₃=0.000, del(AATG)₂=0.000, delAATG=0.000, dupAATG=0.000, dup(AATG)₂=0.000, dup(AATG)₃=0.000, dup(AATG)₄=0.000
Allele Frequency Aggregator	Other	Sub	125	(GAAT)₉G=0.984	del(AATG)₅=0.000, del(AATG)₄=0.000, del(AATG)₃=0.000, del(AATG)₂=0.000, delAATG=0.008, dupAATG=0.008, dup(AATG)₂=0.000, dup(AATG)₃=0.000, dup(AATG)₄=0.000
Allele Frequency Aggregator	Asian	Sub	50	(GAAT)₉G=1.00	del(AATG)₅=0.00, del(AATG)₄=0.00, del(AATG)₃=0.00, del(AATG)₂=0.00, delAATG=0.00, dupAATG=0.00, dup(AATG)₂=0.00, dup(AATG)₃=0.00, dup(AATG)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	48	(GAAT)₉G=1.00	del(AATG)₅=0.00, del(AATG)₄=0.00, del(AATG)₃=0.00, del(AATG)₂=0.00, delAATG=0.00, dupAATG=0.00, dup(AATG)₂=0.00, dup(AATG)₃=0.00, dup(AATG)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(GAAT)₉G=1.00	del(AATG)₅=0.00, del(AATG)₄=0.00, del(AATG)₃=0.00, del(AATG)₂=0.00, delAATG=0.00, dupAATG=0.00, dup(AATG)₂=0.00, dup(AATG)₃=0.00, dup(AATG)₄=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 8	NC_000008.11:g.31136838AATG[4]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[5]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[6]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[7]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[8]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[10]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[11]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[12]
GRCh38.p14 chr 8	NC_000008.11:g.31136838AATG[13]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[4]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[5]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[6]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[7]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[8]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[10]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[11]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[12]
GRCh37.p13 chr 8	NC_000008.10:g.30994354AATG[13]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[4]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[5]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[6]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[7]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[8]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[10]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[11]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[12]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108577AATG[13]

Gene: WRN, WRN RecQ like helicase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
WRN transcript	NM_000553.6:c.2967+4331GA… NM_000553.6:c.2967+4331GAAT[4]	N/A	Intron Variant
WRN transcript variant X1	XM_011544639.4:c.2886+433… XM_011544639.4:c.2886+4331GAAT[4]	N/A	Intron Variant
WRN transcript variant X5	XM_011544640.2:c.1368+433… XM_011544640.2:c.1368+4331GAAT[4]	N/A	Intron Variant
WRN transcript variant X2	XR_949470.4:n.	N/A	Intron Variant
WRN transcript variant X3	XR_949471.4:n.	N/A	Intron Variant
WRN transcript variant X4	XR_949472.4: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	(GAAT)₉G=	del(AATG)₅	del(AATG)₄	del(AATG)₃	del(AATG)₂	delAATG	dupAATG	dup(AATG)₂	dup(AATG)₃	dup(AATG)₄
GRCh38.p14 chr 8	NC_000008.11:g.31136837_31136873=	NC_000008.11:g.31136838AATG[4]	NC_000008.11:g.31136838AATG[5]	NC_000008.11:g.31136838AATG[6]	NC_000008.11:g.31136838AATG[7]	NC_000008.11:g.31136838AATG[8]	NC_000008.11:g.31136838AATG[10]	NC_000008.11:g.31136838AATG[11]	NC_000008.11:g.31136838AATG[12]	NC_000008.11:g.31136838AATG[13]
GRCh37.p13 chr 8	NC_000008.10:g.30994353_30994389=	NC_000008.10:g.30994354AATG[4]	NC_000008.10:g.30994354AATG[5]	NC_000008.10:g.30994354AATG[6]	NC_000008.10:g.30994354AATG[7]	NC_000008.10:g.30994354AATG[8]	NC_000008.10:g.30994354AATG[10]	NC_000008.10:g.30994354AATG[11]	NC_000008.10:g.30994354AATG[12]	NC_000008.10:g.30994354AATG[13]
WRN RefSeqGene (LRG_524)	NG_008870.1:g.108576_108612=	NG_008870.1:g.108577AATG[4]	NG_008870.1:g.108577AATG[5]	NG_008870.1:g.108577AATG[6]	NG_008870.1:g.108577AATG[7]	NG_008870.1:g.108577AATG[8]	NG_008870.1:g.108577AATG[10]	NG_008870.1:g.108577AATG[11]	NG_008870.1:g.108577AATG[12]	NG_008870.1:g.108577AATG[13]
WRN transcript	NM_000553.4:c.2967+4331=	NM_000553.4:c.2967+4331GAAT[4]	NM_000553.4:c.2967+4331GAAT[5]	NM_000553.4:c.2967+4331GAAT[6]	NM_000553.4:c.2967+4331GAAT[7]	NM_000553.4:c.2967+4331GAAT[8]	NM_000553.4:c.2967+4331GAAT[10]	NM_000553.4:c.2967+4331GAAT[11]	NM_000553.4:c.2967+4331GAAT[12]	NM_000553.4:c.2967+4331GAAT[13]
WRN transcript	NM_000553.6:c.2967+4331=	NM_000553.6:c.2967+4331GAAT[4]	NM_000553.6:c.2967+4331GAAT[5]	NM_000553.6:c.2967+4331GAAT[6]	NM_000553.6:c.2967+4331GAAT[7]	NM_000553.6:c.2967+4331GAAT[8]	NM_000553.6:c.2967+4331GAAT[10]	NM_000553.6:c.2967+4331GAAT[11]	NM_000553.6:c.2967+4331GAAT[12]	NM_000553.6:c.2967+4331GAAT[13]
WRN transcript variant X1	XM_005273632.1:c.2886+4331=	XM_005273632.1:c.2886+4331GAAT[4]	XM_005273632.1:c.2886+4331GAAT[5]	XM_005273632.1:c.2886+4331GAAT[6]	XM_005273632.1:c.2886+4331GAAT[7]	XM_005273632.1:c.2886+4331GAAT[8]	XM_005273632.1:c.2886+4331GAAT[10]	XM_005273632.1:c.2886+4331GAAT[11]	XM_005273632.1:c.2886+4331GAAT[12]	XM_005273632.1:c.2886+4331GAAT[13]
WRN transcript variant X1	XM_011544639.4:c.2886+4331=	XM_011544639.4:c.2886+4331GAAT[4]	XM_011544639.4:c.2886+4331GAAT[5]	XM_011544639.4:c.2886+4331GAAT[6]	XM_011544639.4:c.2886+4331GAAT[7]	XM_011544639.4:c.2886+4331GAAT[8]	XM_011544639.4:c.2886+4331GAAT[10]	XM_011544639.4:c.2886+4331GAAT[11]	XM_011544639.4:c.2886+4331GAAT[12]	XM_011544639.4:c.2886+4331GAAT[13]
WRN transcript variant X5	XM_011544640.2:c.1368+4331=	XM_011544640.2:c.1368+4331GAAT[4]	XM_011544640.2:c.1368+4331GAAT[5]	XM_011544640.2:c.1368+4331GAAT[6]	XM_011544640.2:c.1368+4331GAAT[7]	XM_011544640.2:c.1368+4331GAAT[8]	XM_011544640.2:c.1368+4331GAAT[10]	XM_011544640.2:c.1368+4331GAAT[11]	XM_011544640.2:c.1368+4331GAAT[12]	XM_011544640.2:c.1368+4331GAAT[13]

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#.

70 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79876945	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95488847	Feb 05, 2009 (130)
3	BCMHGSC_JDW	ss103766134	Dec 01, 2009 (131)
4	GMI	ss288900535	May 04, 2012 (137)
5	GMI	ss288900536	May 04, 2012 (138)
6	1000GENOMES	ss327038567	May 09, 2011 (134)
7	1000GENOMES	ss327099570	Jan 10, 2018 (151)
8	1000GENOMES	ss327418676	Jan 10, 2018 (151)
9	LUNTER	ss551833635	Apr 25, 2013 (138)
10	LUNTER	ss552051254	Apr 25, 2013 (138)
11	LUNTER	ss553336053	Apr 25, 2013 (138)
12	SSMP	ss663848683	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666433706	Apr 25, 2013 (138)
14	1000GENOMES	ss1367890415	Aug 21, 2014 (142)
15	1000GENOMES	ss1367890416	Aug 21, 2014 (142)
16	1000GENOMES	ss1367890417	Aug 21, 2014 (142)
17	1000GENOMES	ss1367890418	Aug 21, 2014 (142)
18	SWEGEN	ss3002941337	Nov 08, 2017 (151)
19	MCHAISSO	ss3066195869	Jan 10, 2018 (151)
20	BEROUKHIMLAB	ss3644259255	Oct 12, 2018 (152)
21	URBANLAB	ss3648887040	Oct 12, 2018 (152)
22	EVA_DECODE	ss3721729645	Jul 13, 2019 (153)
23	EVA_DECODE	ss3721729646	Jul 13, 2019 (153)
24	EVA_DECODE	ss3721729647	Jul 13, 2019 (153)
25	EVA_DECODE	ss3721729648	Jul 13, 2019 (153)
26	PACBIO	ss3786109943	Jul 13, 2019 (153)
27	PACBIO	ss3786109944	Jul 13, 2019 (153)
28	PACBIO	ss3791372862	Jul 13, 2019 (153)
29	PACBIO	ss3791372863	Jul 13, 2019 (153)
30	PACBIO	ss3796254120	Jul 13, 2019 (153)
31	PACBIO	ss3796254121	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3810986984	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3810986986	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3810986987	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3810986988	Jul 13, 2019 (153)
36	EVA	ss3839059286	Apr 26, 2020 (154)
37	EVA	ss3844517709	Apr 26, 2020 (154)
38	KOGIC	ss3963577844	Apr 26, 2020 (154)
39	KOGIC	ss3963577845	Apr 26, 2020 (154)
40	KOGIC	ss3963577846	Apr 26, 2020 (154)
41	KOGIC	ss3963577847	Apr 26, 2020 (154)
42	KOGIC	ss3963577848	Apr 26, 2020 (154)
43	GNOMAD	ss4181779175	Apr 26, 2021 (155)
44	GNOMAD	ss4181779176	Apr 26, 2021 (155)
45	GNOMAD	ss4181779177	Apr 26, 2021 (155)
46	GNOMAD	ss4181779178	Apr 26, 2021 (155)
47	GNOMAD	ss4181779179	Apr 26, 2021 (155)
48	GNOMAD	ss4181779180	Apr 26, 2021 (155)
49	GNOMAD	ss4181779181	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5188036945	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5188036946	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5188036947	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5188036948	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5188036949	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5188036950	Apr 26, 2021 (155)
56	1000G_HIGH_COVERAGE	ss5276630051	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5276630053	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5276630054	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5276630055	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5276630056	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5473253239	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5473253240	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5473253242	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5729765371	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5729765372	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5729765373	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5729765374	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5729765376	Oct 16, 2022 (156)
69	EVA	ss5830340873	Oct 16, 2022 (156)
70	EVA	ss5830340874	Oct 16, 2022 (156)
71	1000Genomes Submission ignored due to conflicting rows: Row 41363425 (NC_000008.10:30994352::GAATGAAT 118/5008) Row 41363426 (NC_000008.10:30994352::GAATGAATGAAT 6/5008) Row 41363427 (NC_000008.10:30994352:GAAT: 851/3840)	-	Oct 12, 2018 (152)
72	1000Genomes Submission ignored due to conflicting rows: Row 41363425 (NC_000008.10:30994352::GAATGAAT 118/5008) Row 41363426 (NC_000008.10:30994352::GAATGAATGAAT 6/5008) Row 41363427 (NC_000008.10:30994352:GAAT: 851/3840)	-	Oct 12, 2018 (152)
73	1000Genomes Submission ignored due to conflicting rows: Row 41363425 (NC_000008.10:30994352::GAATGAAT 118/5008) Row 41363426 (NC_000008.10:30994352::GAATGAATGAAT 6/5008) Row 41363427 (NC_000008.10:30994352:GAAT: 851/3840)	-	Oct 12, 2018 (152)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291637195 (NC_000008.11:31136836::GAAT 34868/137628) Row 291637196 (NC_000008.11:31136836::GAATGAAT 4217/137760) Row 291637197 (NC_000008.11:31136836::GAATGAATGAAT 66/137774)...	-	Apr 26, 2021 (155)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 19955845 (NC_000008.11:31136844:GAAT: 105/1832) Row 19955846 (NC_000008.11:31136848::GAAT 555/1832) Row 19955847 (NC_000008.11:31136848::GAATGAAT 3/1832)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 19955845 (NC_000008.11:31136844:GAAT: 105/1832) Row 19955846 (NC_000008.11:31136848::GAAT 555/1832) Row 19955847 (NC_000008.11:31136848::GAATGAAT 3/1832)...	-	Apr 26, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 19955845 (NC_000008.11:31136844:GAAT: 105/1832) Row 19955846 (NC_000008.11:31136848::GAAT 555/1832) Row 19955847 (NC_000008.11:31136848::GAATGAAT 3/1832)...	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 19955845 (NC_000008.11:31136844:GAAT: 105/1832) Row 19955846 (NC_000008.11:31136848::GAAT 555/1832) Row 19955847 (NC_000008.11:31136848::GAATGAAT 3/1832)...	-	Apr 26, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 19955845 (NC_000008.11:31136844:GAAT: 105/1832) Row 19955846 (NC_000008.11:31136848::GAAT 555/1832) Row 19955847 (NC_000008.11:31136848::GAATGAAT 3/1832)...	-	Apr 26, 2020 (154)
86	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 46006252 (NC_000008.10:30994352::GAAT 6159/16760) Row 46006253 (NC_000008.10:30994352:GAAT: 568/16760) Row 46006254 (NC_000008.10:30994352::GAATGAAT 44/16760)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 63602475 (NC_000008.11:31136836::GAAT 10444/28258) Row 63602476 (NC_000008.11:31136836:GAAT: 999/28258) Row 63602477 (NC_000008.11:31136836::GAATGAAT 77/28258)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 63602475 (NC_000008.11:31136836::GAAT 10444/28258) Row 63602476 (NC_000008.11:31136836:GAAT: 999/28258) Row 63602477 (NC_000008.11:31136836::GAATGAAT 77/28258)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 63602475 (NC_000008.11:31136836::GAAT 10444/28258) Row 63602476 (NC_000008.11:31136836:GAAT: 999/28258) Row 63602477 (NC_000008.11:31136836::GAATGAAT 77/28258)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 63602475 (NC_000008.11:31136836::GAAT 10444/28258) Row 63602476 (NC_000008.11:31136836:GAAT: 999/28258) Row 63602477 (NC_000008.11:31136836::GAATGAAT 77/28258)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 63602475 (NC_000008.11:31136836::GAAT 10444/28258) Row 63602476 (NC_000008.11:31136836:GAAT: 999/28258) Row 63602477 (NC_000008.11:31136836::GAATGAAT 77/28258)...	-	Oct 16, 2022 (156)
97	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 5127994 (NC_000008.10:30994352::GAATGAAT 1/162) Row 5127995 (NC_000008.10:30994352:GAAT: 9/170) Row 5127996 (NC_000008.10:30994352::GAAT 43/204)	-	Jul 13, 2019 (153)
98	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 5127994 (NC_000008.10:30994352::GAATGAAT 1/162) Row 5127995 (NC_000008.10:30994352:GAAT: 9/170) Row 5127996 (NC_000008.10:30994352::GAAT 43/204)	-	Jul 13, 2019 (153)
99	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 5127994 (NC_000008.10:30994352::GAATGAAT 1/162) Row 5127995 (NC_000008.10:30994352:GAAT: 9/170) Row 5127996 (NC_000008.10:30994352::GAAT 43/204)	-	Jul 13, 2019 (153)
100	ALFA	NC_000008.11 - 31136837	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)
rs199630255	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATG	(self)
ss4181779181	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATG	(self)
ss5188036948	NC_000008.10:30994352:GAATGAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATG	(self)
ss3963577847, ss4181779180	NC_000008.11:31136836:GAATGAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATG	(self)
ss3002941337, ss5188036950	NC_000008.10:30994352:GAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATG	(self)
ss3721729648, ss4181779179, ss5276630056, ss5729765376	NC_000008.11:31136836:GAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATG	(self)
ss3963577848	NC_000008.11:31136840:GAATGAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATG	(self)
ss288900535, ss327099570, ss327418676	NC_000008.9:31113894:GAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss666433706, ss1367890417, ss3786109943, ss3791372862, ss3796254120, ss5188036946, ss5830340874	NC_000008.10:30994352:GAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3810986988, ss4181779178, ss5276630051, ss5473253240, ss5729765372	NC_000008.11:31136836:GAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3721729647	NC_000008.11:31136840:GAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3963577844	NC_000008.11:31136844:GAAT:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss103766134	NT_167187.1:18852531:AATG:	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss327038567, ss551833635, ss552051254, ss553336053	NC_000008.9:31113894::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss288900536	NC_000008.9:31113931::AATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss663848683, ss3644259255, ss3786109944, ss3791372863, ss3796254121, ss5188036945, ss5830340873	NC_000008.10:30994352::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss1367890418, ss3839059286	NC_000008.10:30994356::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3066195869, ss4181779175, ss5276630053, ss5473253239, ss5729765371	NC_000008.11:31136836::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3810986987, ss3844517709	NC_000008.11:31136840::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3721729646	NC_000008.11:31136844::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3648887040, ss3963577845	NC_000008.11:31136848::GAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss95488847	NT_167187.1:18852535::AATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss1367890415, ss5188036947	NC_000008.10:30994352::GAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3810986986, ss4181779176, ss5276630054, ss5473253242, ss5729765373	NC_000008.11:31136836::GAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3810986984	NC_000008.11:31136840::GAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3721729645	NC_000008.11:31136844::GAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss3963577846	NC_000008.11:31136848::GAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss79876945	NT_167187.1:18852535::AATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss1367890416, ss5188036949	NC_000008.10:30994352::GAATGAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
ss4181779177, ss5276630055, ss5729765374	NC_000008.11:31136836::GAATGAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)
3737267617	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3558074720	NC_000008.11:31136836::GAATGAATGAA… NC_000008.11:31136836::GAATGAATGAATGAAT	NC_000008.11:31136836:GAATGAATGAAT… NC_000008.11:31136836:GAATGAATGAATGAATGAATGAATGAATGAATGAATG:GAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATG

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

No publications for rs60617461

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs60617461