Name: rs60350092
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.

rs60350092

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:20184927-20184936 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.1656 (1197/7230, ALFA)
dupA=0.1524 (763/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SGO1 : Intron Variant
SGO1-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	7230	AAAAAAAAAA=0.6949	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAA=0.1656, AAAAAAAAAAA=0.0497, AAAAAAAAAAAAA=0.0896, AAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	0.726374	0.063736	0.20989	32
European	Sub	6678	AAAAAAAAAA=0.6704	AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAA=0.1785, AAAAAAAAAAA=0.0538, AAAAAAAAAAAAA=0.0970, AAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	0.697229	0.070497	0.232274	32
African	Sub	344	AAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	AAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	332	AAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAA=0	AAAAAAA=0, AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	54	AAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	60	AAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	AAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	86	AAAAAAAAAA=0.94	AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.06, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	0.906977	0.023256	0.069767	4

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	7230	(A)₁₀=0.6949	delAAA=0.0000, delAA=0.0000, delA=0.1656, dupA=0.0497, dupAA=0.0000, dupAAA=0.0896, dup(A)₄=0.0003, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	6678	(A)₁₀=0.6704	delAAA=0.0000, delAA=0.0000, delA=0.1785, dupA=0.0538, dupAA=0.0000, dupAAA=0.0970, dup(A)₄=0.0003, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	344	(A)₁₀=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	86	(A)₁₀=0.94	delAAA=0.00, delAA=0.00, delA=0.06, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	60	(A)₁₀=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	54	(A)₁₀=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(A)₁₀=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₀=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.1524, dupAAA=0.0749
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.2163, dupAAA=0.0083
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.1865, dupAAA=0.0089
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.1113, dupAAA=0.1511
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.105, dupAAA=0.084
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.107, dupAAA=0.174

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.20184934_20184936del
GRCh38.p14 chr 3	NC_000003.12:g.20184935_20184936del
GRCh38.p14 chr 3	NC_000003.12:g.20184936del
GRCh38.p14 chr 3	NC_000003.12:g.20184936dup
GRCh38.p14 chr 3	NC_000003.12:g.20184935_20184936dup
GRCh38.p14 chr 3	NC_000003.12:g.20184934_20184936dup
GRCh38.p14 chr 3	NC_000003.12:g.20184933_20184936dup
GRCh38.p14 chr 3	NC_000003.12:g.20184932_20184936dup
GRCh37.p13 chr 3	NC_000003.11:g.20226426_20226428del
GRCh37.p13 chr 3	NC_000003.11:g.20226427_20226428del
GRCh37.p13 chr 3	NC_000003.11:g.20226428del
GRCh37.p13 chr 3	NC_000003.11:g.20226428dup
GRCh37.p13 chr 3	NC_000003.11:g.20226427_20226428dup
GRCh37.p13 chr 3	NC_000003.11:g.20226426_20226428dup
GRCh37.p13 chr 3	NC_000003.11:g.20226425_20226428dup
GRCh37.p13 chr 3	NC_000003.11:g.20226424_20226428dup
SGO1 RefSeqGene	NG_042062.1:g.6303_6305del
SGO1 RefSeqGene	NG_042062.1:g.6304_6305del
SGO1 RefSeqGene	NG_042062.1:g.6305del
SGO1 RefSeqGene	NG_042062.1:g.6305dup
SGO1 RefSeqGene	NG_042062.1:g.6304_6305dup
SGO1 RefSeqGene	NG_042062.1:g.6303_6305dup
SGO1 RefSeqGene	NG_042062.1:g.6302_6305dup
SGO1 RefSeqGene	NG_042062.1:g.6301_6305dup

Gene: SGO1, shugoshin 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SGO1 transcript variant A1	NM_001012409.4:c.-7-895_-… NM_001012409.4:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1F	NM_001012410.5:c.-7-895_-… NM_001012410.5:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1C	NM_001012411.4:c.-7-895_-… NM_001012411.4:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1H	NM_001012412.5:c.-7-895_-… NM_001012412.5:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1B	NM_001012413.4:c.-7-895_-… NM_001012413.4:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant 1	NM_001199251.3:c.-7-895_-… NM_001199251.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1E	NM_001199252.3:c.-7-895_-… NM_001199252.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1D	NM_001199253.3:c.-7-895_-… NM_001199253.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1G	NM_001199254.3:c.-7-895_-… NM_001199254.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1A	NM_001199255.3:c.-7-895_-… NM_001199255.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1K	NM_001199256.3:c.-7-895_-… NM_001199256.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1J	NM_001199257.3:c.-7-895_-… NM_001199257.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant Sgo1L	NM_138484.5:c.-7-895_-7-8… NM_138484.5:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant 14	NR_131179.2:n.	N/A	Intron Variant
SGO1 transcript variant 15	NR_131180.2:n.	N/A	Intron Variant
SGO1 transcript variant X1	XM_011533373.3:c.-7-895_-… XM_011533373.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant X3	XM_011533375.3:c.-8+383_-… XM_011533375.3:c.-8+383_-8+385del	N/A	Intron Variant
SGO1 transcript variant X2	XM_011533376.3:c.-8+528_-… XM_011533376.3:c.-8+528_-8+530del	N/A	Intron Variant
SGO1 transcript variant X4	XM_011533377.3:c.-7-895_-… XM_011533377.3:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant X5	XM_047447486.1:c.-7-895_-… XM_047447486.1:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant X6	XM_047447487.1:c.-8+383_-… XM_047447487.1:c.-8+383_-8+385del	N/A	Intron Variant
SGO1 transcript variant X7	XM_047447488.1:c.-8+383_-… XM_047447488.1:c.-8+383_-8+385del	N/A	Intron Variant
SGO1 transcript variant X8	XM_047447489.1:c.-7-895_-… XM_047447489.1:c.-7-895_-7-893del	N/A	Intron Variant
SGO1 transcript variant X9	XM_047447490.1:c.-8+528_-… XM_047447490.1:c.-8+528_-8+530del	N/A	Intron Variant

Gene: SGO1-AS1, SGO1 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SGO1-AS1 transcript	NR_132785.1: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)₁₀=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 3	NC_000003.12:g.20184927_20184936=	NC_000003.12:g.20184934_20184936del	NC_000003.12:g.20184935_20184936del	NC_000003.12:g.20184936del	NC_000003.12:g.20184936dup	NC_000003.12:g.20184935_20184936dup	NC_000003.12:g.20184934_20184936dup	NC_000003.12:g.20184933_20184936dup	NC_000003.12:g.20184932_20184936dup
GRCh37.p13 chr 3	NC_000003.11:g.20226419_20226428=	NC_000003.11:g.20226426_20226428del	NC_000003.11:g.20226427_20226428del	NC_000003.11:g.20226428del	NC_000003.11:g.20226428dup	NC_000003.11:g.20226427_20226428dup	NC_000003.11:g.20226426_20226428dup	NC_000003.11:g.20226425_20226428dup	NC_000003.11:g.20226424_20226428dup
SGO1 RefSeqGene	NG_042062.1:g.6296_6305=	NG_042062.1:g.6303_6305del	NG_042062.1:g.6304_6305del	NG_042062.1:g.6305del	NG_042062.1:g.6305dup	NG_042062.1:g.6304_6305dup	NG_042062.1:g.6303_6305dup	NG_042062.1:g.6302_6305dup	NG_042062.1:g.6301_6305dup
SGOL1 transcript variant A1	NM_001012409.2:c.-7-893=	NM_001012409.2:c.-7-895_-7-893del	NM_001012409.2:c.-7-894_-7-893del	NM_001012409.2:c.-7-893del	NM_001012409.2:c.-7-893dup	NM_001012409.2:c.-7-894_-7-893dup	NM_001012409.2:c.-7-895_-7-893dup	NM_001012409.2:c.-7-896_-7-893dup	NM_001012409.2:c.-7-897_-7-893dup
SGO1 transcript variant A1	NM_001012409.4:c.-7-893=	NM_001012409.4:c.-7-895_-7-893del	NM_001012409.4:c.-7-894_-7-893del	NM_001012409.4:c.-7-893del	NM_001012409.4:c.-7-893dup	NM_001012409.4:c.-7-894_-7-893dup	NM_001012409.4:c.-7-895_-7-893dup	NM_001012409.4:c.-7-896_-7-893dup	NM_001012409.4:c.-7-897_-7-893dup
SGOL1 transcript variant A2	NM_001012410.3:c.-7-893=	NM_001012410.3:c.-7-895_-7-893del	NM_001012410.3:c.-7-894_-7-893del	NM_001012410.3:c.-7-893del	NM_001012410.3:c.-7-893dup	NM_001012410.3:c.-7-894_-7-893dup	NM_001012410.3:c.-7-895_-7-893dup	NM_001012410.3:c.-7-896_-7-893dup	NM_001012410.3:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1F	NM_001012410.5:c.-7-893=	NM_001012410.5:c.-7-895_-7-893del	NM_001012410.5:c.-7-894_-7-893del	NM_001012410.5:c.-7-893del	NM_001012410.5:c.-7-893dup	NM_001012410.5:c.-7-894_-7-893dup	NM_001012410.5:c.-7-895_-7-893dup	NM_001012410.5:c.-7-896_-7-893dup	NM_001012410.5:c.-7-897_-7-893dup
SGOL1 transcript variant B1	NM_001012411.2:c.-7-893=	NM_001012411.2:c.-7-895_-7-893del	NM_001012411.2:c.-7-894_-7-893del	NM_001012411.2:c.-7-893del	NM_001012411.2:c.-7-893dup	NM_001012411.2:c.-7-894_-7-893dup	NM_001012411.2:c.-7-895_-7-893dup	NM_001012411.2:c.-7-896_-7-893dup	NM_001012411.2:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1C	NM_001012411.4:c.-7-893=	NM_001012411.4:c.-7-895_-7-893del	NM_001012411.4:c.-7-894_-7-893del	NM_001012411.4:c.-7-893del	NM_001012411.4:c.-7-893dup	NM_001012411.4:c.-7-894_-7-893dup	NM_001012411.4:c.-7-895_-7-893dup	NM_001012411.4:c.-7-896_-7-893dup	NM_001012411.4:c.-7-897_-7-893dup
SGOL1 transcript variant B2	NM_001012412.3:c.-7-893=	NM_001012412.3:c.-7-895_-7-893del	NM_001012412.3:c.-7-894_-7-893del	NM_001012412.3:c.-7-893del	NM_001012412.3:c.-7-893dup	NM_001012412.3:c.-7-894_-7-893dup	NM_001012412.3:c.-7-895_-7-893dup	NM_001012412.3:c.-7-896_-7-893dup	NM_001012412.3:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1H	NM_001012412.5:c.-7-893=	NM_001012412.5:c.-7-895_-7-893del	NM_001012412.5:c.-7-894_-7-893del	NM_001012412.5:c.-7-893del	NM_001012412.5:c.-7-893dup	NM_001012412.5:c.-7-894_-7-893dup	NM_001012412.5:c.-7-895_-7-893dup	NM_001012412.5:c.-7-896_-7-893dup	NM_001012412.5:c.-7-897_-7-893dup
SGOL1 transcript variant C1	NM_001012413.2:c.-7-893=	NM_001012413.2:c.-7-895_-7-893del	NM_001012413.2:c.-7-894_-7-893del	NM_001012413.2:c.-7-893del	NM_001012413.2:c.-7-893dup	NM_001012413.2:c.-7-894_-7-893dup	NM_001012413.2:c.-7-895_-7-893dup	NM_001012413.2:c.-7-896_-7-893dup	NM_001012413.2:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1B	NM_001012413.4:c.-7-893=	NM_001012413.4:c.-7-895_-7-893del	NM_001012413.4:c.-7-894_-7-893del	NM_001012413.4:c.-7-893del	NM_001012413.4:c.-7-893dup	NM_001012413.4:c.-7-894_-7-893dup	NM_001012413.4:c.-7-895_-7-893dup	NM_001012413.4:c.-7-896_-7-893dup	NM_001012413.4:c.-7-897_-7-893dup
SGOL1 transcript variant A3	NM_001199251.1:c.-7-893=	NM_001199251.1:c.-7-895_-7-893del	NM_001199251.1:c.-7-894_-7-893del	NM_001199251.1:c.-7-893del	NM_001199251.1:c.-7-893dup	NM_001199251.1:c.-7-894_-7-893dup	NM_001199251.1:c.-7-895_-7-893dup	NM_001199251.1:c.-7-896_-7-893dup	NM_001199251.1:c.-7-897_-7-893dup
SGO1 transcript variant 1	NM_001199251.3:c.-7-893=	NM_001199251.3:c.-7-895_-7-893del	NM_001199251.3:c.-7-894_-7-893del	NM_001199251.3:c.-7-893del	NM_001199251.3:c.-7-893dup	NM_001199251.3:c.-7-894_-7-893dup	NM_001199251.3:c.-7-895_-7-893dup	NM_001199251.3:c.-7-896_-7-893dup	NM_001199251.3:c.-7-897_-7-893dup
SGOL1 transcript variant A4	NM_001199252.1:c.-7-893=	NM_001199252.1:c.-7-895_-7-893del	NM_001199252.1:c.-7-894_-7-893del	NM_001199252.1:c.-7-893del	NM_001199252.1:c.-7-893dup	NM_001199252.1:c.-7-894_-7-893dup	NM_001199252.1:c.-7-895_-7-893dup	NM_001199252.1:c.-7-896_-7-893dup	NM_001199252.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1E	NM_001199252.3:c.-7-893=	NM_001199252.3:c.-7-895_-7-893del	NM_001199252.3:c.-7-894_-7-893del	NM_001199252.3:c.-7-893del	NM_001199252.3:c.-7-893dup	NM_001199252.3:c.-7-894_-7-893dup	NM_001199252.3:c.-7-895_-7-893dup	NM_001199252.3:c.-7-896_-7-893dup	NM_001199252.3:c.-7-897_-7-893dup
SGOL1 transcript variant B3	NM_001199253.1:c.-7-893=	NM_001199253.1:c.-7-895_-7-893del	NM_001199253.1:c.-7-894_-7-893del	NM_001199253.1:c.-7-893del	NM_001199253.1:c.-7-893dup	NM_001199253.1:c.-7-894_-7-893dup	NM_001199253.1:c.-7-895_-7-893dup	NM_001199253.1:c.-7-896_-7-893dup	NM_001199253.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1D	NM_001199253.3:c.-7-893=	NM_001199253.3:c.-7-895_-7-893del	NM_001199253.3:c.-7-894_-7-893del	NM_001199253.3:c.-7-893del	NM_001199253.3:c.-7-893dup	NM_001199253.3:c.-7-894_-7-893dup	NM_001199253.3:c.-7-895_-7-893dup	NM_001199253.3:c.-7-896_-7-893dup	NM_001199253.3:c.-7-897_-7-893dup
SGOL1 transcript variant B4	NM_001199254.1:c.-7-893=	NM_001199254.1:c.-7-895_-7-893del	NM_001199254.1:c.-7-894_-7-893del	NM_001199254.1:c.-7-893del	NM_001199254.1:c.-7-893dup	NM_001199254.1:c.-7-894_-7-893dup	NM_001199254.1:c.-7-895_-7-893dup	NM_001199254.1:c.-7-896_-7-893dup	NM_001199254.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1G	NM_001199254.3:c.-7-893=	NM_001199254.3:c.-7-895_-7-893del	NM_001199254.3:c.-7-894_-7-893del	NM_001199254.3:c.-7-893del	NM_001199254.3:c.-7-893dup	NM_001199254.3:c.-7-894_-7-893dup	NM_001199254.3:c.-7-895_-7-893dup	NM_001199254.3:c.-7-896_-7-893dup	NM_001199254.3:c.-7-897_-7-893dup
SGOL1 transcript variant C3	NM_001199255.1:c.-7-893=	NM_001199255.1:c.-7-895_-7-893del	NM_001199255.1:c.-7-894_-7-893del	NM_001199255.1:c.-7-893del	NM_001199255.1:c.-7-893dup	NM_001199255.1:c.-7-894_-7-893dup	NM_001199255.1:c.-7-895_-7-893dup	NM_001199255.1:c.-7-896_-7-893dup	NM_001199255.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1A	NM_001199255.3:c.-7-893=	NM_001199255.3:c.-7-895_-7-893del	NM_001199255.3:c.-7-894_-7-893del	NM_001199255.3:c.-7-893del	NM_001199255.3:c.-7-893dup	NM_001199255.3:c.-7-894_-7-893dup	NM_001199255.3:c.-7-895_-7-893dup	NM_001199255.3:c.-7-896_-7-893dup	NM_001199255.3:c.-7-897_-7-893dup
SGOL1 transcript variant C4	NM_001199256.1:c.-7-893=	NM_001199256.1:c.-7-895_-7-893del	NM_001199256.1:c.-7-894_-7-893del	NM_001199256.1:c.-7-893del	NM_001199256.1:c.-7-893dup	NM_001199256.1:c.-7-894_-7-893dup	NM_001199256.1:c.-7-895_-7-893dup	NM_001199256.1:c.-7-896_-7-893dup	NM_001199256.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1K	NM_001199256.3:c.-7-893=	NM_001199256.3:c.-7-895_-7-893del	NM_001199256.3:c.-7-894_-7-893del	NM_001199256.3:c.-7-893del	NM_001199256.3:c.-7-893dup	NM_001199256.3:c.-7-894_-7-893dup	NM_001199256.3:c.-7-895_-7-893dup	NM_001199256.3:c.-7-896_-7-893dup	NM_001199256.3:c.-7-897_-7-893dup
SGOL1 transcript variant D1	NM_001199257.1:c.-7-893=	NM_001199257.1:c.-7-895_-7-893del	NM_001199257.1:c.-7-894_-7-893del	NM_001199257.1:c.-7-893del	NM_001199257.1:c.-7-893dup	NM_001199257.1:c.-7-894_-7-893dup	NM_001199257.1:c.-7-895_-7-893dup	NM_001199257.1:c.-7-896_-7-893dup	NM_001199257.1:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1J	NM_001199257.3:c.-7-893=	NM_001199257.3:c.-7-895_-7-893del	NM_001199257.3:c.-7-894_-7-893del	NM_001199257.3:c.-7-893del	NM_001199257.3:c.-7-893dup	NM_001199257.3:c.-7-894_-7-893dup	NM_001199257.3:c.-7-895_-7-893dup	NM_001199257.3:c.-7-896_-7-893dup	NM_001199257.3:c.-7-897_-7-893dup
SGOL1 transcript variant C2	NM_138484.3:c.-7-893=	NM_138484.3:c.-7-895_-7-893del	NM_138484.3:c.-7-894_-7-893del	NM_138484.3:c.-7-893del	NM_138484.3:c.-7-893dup	NM_138484.3:c.-7-894_-7-893dup	NM_138484.3:c.-7-895_-7-893dup	NM_138484.3:c.-7-896_-7-893dup	NM_138484.3:c.-7-897_-7-893dup
SGO1 transcript variant Sgo1L	NM_138484.5:c.-7-893=	NM_138484.5:c.-7-895_-7-893del	NM_138484.5:c.-7-894_-7-893del	NM_138484.5:c.-7-893del	NM_138484.5:c.-7-893dup	NM_138484.5:c.-7-894_-7-893dup	NM_138484.5:c.-7-895_-7-893dup	NM_138484.5:c.-7-896_-7-893dup	NM_138484.5:c.-7-897_-7-893dup
SGO1 transcript variant X1	XM_011533373.3:c.-7-893=	XM_011533373.3:c.-7-895_-7-893del	XM_011533373.3:c.-7-894_-7-893del	XM_011533373.3:c.-7-893del	XM_011533373.3:c.-7-893dup	XM_011533373.3:c.-7-894_-7-893dup	XM_011533373.3:c.-7-895_-7-893dup	XM_011533373.3:c.-7-896_-7-893dup	XM_011533373.3:c.-7-897_-7-893dup
SGO1 transcript variant X3	XM_011533375.3:c.-8+385=	XM_011533375.3:c.-8+383_-8+385del	XM_011533375.3:c.-8+384_-8+385del	XM_011533375.3:c.-8+385del	XM_011533375.3:c.-8+385dup	XM_011533375.3:c.-8+384_-8+385dup	XM_011533375.3:c.-8+383_-8+385dup	XM_011533375.3:c.-8+382_-8+385dup	XM_011533375.3:c.-8+381_-8+385dup
SGO1 transcript variant X2	XM_011533376.3:c.-8+530=	XM_011533376.3:c.-8+528_-8+530del	XM_011533376.3:c.-8+529_-8+530del	XM_011533376.3:c.-8+530del	XM_011533376.3:c.-8+530dup	XM_011533376.3:c.-8+529_-8+530dup	XM_011533376.3:c.-8+528_-8+530dup	XM_011533376.3:c.-8+527_-8+530dup	XM_011533376.3:c.-8+526_-8+530dup
SGO1 transcript variant X4	XM_011533377.3:c.-7-893=	XM_011533377.3:c.-7-895_-7-893del	XM_011533377.3:c.-7-894_-7-893del	XM_011533377.3:c.-7-893del	XM_011533377.3:c.-7-893dup	XM_011533377.3:c.-7-894_-7-893dup	XM_011533377.3:c.-7-895_-7-893dup	XM_011533377.3:c.-7-896_-7-893dup	XM_011533377.3:c.-7-897_-7-893dup
SGO1 transcript variant X5	XM_047447486.1:c.-7-893=	XM_047447486.1:c.-7-895_-7-893del	XM_047447486.1:c.-7-894_-7-893del	XM_047447486.1:c.-7-893del	XM_047447486.1:c.-7-893dup	XM_047447486.1:c.-7-894_-7-893dup	XM_047447486.1:c.-7-895_-7-893dup	XM_047447486.1:c.-7-896_-7-893dup	XM_047447486.1:c.-7-897_-7-893dup
SGO1 transcript variant X6	XM_047447487.1:c.-8+385=	XM_047447487.1:c.-8+383_-8+385del	XM_047447487.1:c.-8+384_-8+385del	XM_047447487.1:c.-8+385del	XM_047447487.1:c.-8+385dup	XM_047447487.1:c.-8+384_-8+385dup	XM_047447487.1:c.-8+383_-8+385dup	XM_047447487.1:c.-8+382_-8+385dup	XM_047447487.1:c.-8+381_-8+385dup
SGO1 transcript variant X7	XM_047447488.1:c.-8+385=	XM_047447488.1:c.-8+383_-8+385del	XM_047447488.1:c.-8+384_-8+385del	XM_047447488.1:c.-8+385del	XM_047447488.1:c.-8+385dup	XM_047447488.1:c.-8+384_-8+385dup	XM_047447488.1:c.-8+383_-8+385dup	XM_047447488.1:c.-8+382_-8+385dup	XM_047447488.1:c.-8+381_-8+385dup
SGO1 transcript variant X8	XM_047447489.1:c.-7-893=	XM_047447489.1:c.-7-895_-7-893del	XM_047447489.1:c.-7-894_-7-893del	XM_047447489.1:c.-7-893del	XM_047447489.1:c.-7-893dup	XM_047447489.1:c.-7-894_-7-893dup	XM_047447489.1:c.-7-895_-7-893dup	XM_047447489.1:c.-7-896_-7-893dup	XM_047447489.1:c.-7-897_-7-893dup
SGO1 transcript variant X9	XM_047447490.1:c.-8+530=	XM_047447490.1:c.-8+528_-8+530del	XM_047447490.1:c.-8+529_-8+530del	XM_047447490.1:c.-8+530del	XM_047447490.1:c.-8+530dup	XM_047447490.1:c.-8+529_-8+530dup	XM_047447490.1:c.-8+528_-8+530dup	XM_047447490.1:c.-8+527_-8+530dup	XM_047447490.1:c.-8+526_-8+530dup

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#.

76 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80543279	Sep 08, 2015 (146)
2	HGSV	ss81187864	Sep 08, 2015 (146)
3	GMI	ss154749675	Dec 01, 2009 (137)
4	BUSHMAN	ss193661176	Jul 04, 2010 (132)
5	GMI	ss287721447	Dec 06, 2013 (138)
6	GMI	ss288329852	May 04, 2012 (137)
7	GMI	ss288329854	May 04, 2012 (138)
8	PJP	ss295090657	May 09, 2011 (137)
9	1000GENOMES	ss326345767	May 09, 2011 (137)
10	1000GENOMES	ss326368211	Jan 10, 2018 (151)
11	1000GENOMES	ss326475152	May 09, 2011 (137)
12	LUNTER	ss551212877	Apr 25, 2013 (138)
13	LUNTER	ss551290194	Apr 25, 2013 (138)
14	LUNTER	ss553003666	Apr 25, 2013 (138)
15	SSMP	ss663395867	Apr 01, 2015 (144)
16	BILGI_BIOE	ss666199133	Apr 25, 2013 (138)
17	1000GENOMES	ss1370058098	Aug 21, 2014 (142)
18	1000GENOMES	ss1370058101	Aug 21, 2014 (142)
19	EVA_UK10K_TWINSUK	ss1703536637	Apr 01, 2015 (144)
20	EVA_UK10K_ALSPAC	ss1703536638	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1710070102	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1710070117	Apr 01, 2015 (144)
23	HAMMER_LAB	ss1798956504	Sep 08, 2015 (146)
24	HAMMER_LAB	ss1798956507	Sep 08, 2015 (146)
25	SWEGEN	ss2991932370	Jan 10, 2018 (151)
26	MCHAISSO	ss3064899023	Nov 08, 2017 (151)
27	BIOINF_KMB_FNS_UNIBA	ss3645700172	Oct 12, 2018 (152)
28	EVA_DECODE	ss3708764143	Jul 13, 2019 (153)
29	EVA_DECODE	ss3708764144	Jul 13, 2019 (153)
30	EVA_DECODE	ss3708764145	Jul 13, 2019 (153)
31	EVA_DECODE	ss3708764146	Jul 13, 2019 (153)
32	EVA_DECODE	ss3708764147	Jul 13, 2019 (153)
33	ACPOP	ss3729686427	Jul 13, 2019 (153)
34	ACPOP	ss3729686428	Jul 13, 2019 (153)
35	ACPOP	ss3729686429	Jul 13, 2019 (153)
36	INMEGENXS	ss3745654194	Jul 13, 2019 (153)
37	INMEGENXS	ss3745654195	Jul 13, 2019 (153)
38	PACBIO	ss3784251729	Jul 13, 2019 (153)
39	PACBIO	ss3789777640	Jul 13, 2019 (153)
40	PACBIO	ss3794651411	Jul 13, 2019 (153)
41	KHV_HUMAN_GENOMES	ss3802888043	Jul 13, 2019 (153)
42	KHV_HUMAN_GENOMES	ss3802888044	Jul 13, 2019 (153)
43	KHV_HUMAN_GENOMES	ss3802888045	Jul 13, 2019 (153)
44	KHV_HUMAN_GENOMES	ss3802888046	Jul 13, 2019 (153)
45	EVA	ss3827692183	Apr 25, 2020 (154)
46	GNOMAD	ss4066942831	Apr 26, 2021 (155)
47	GNOMAD	ss4066942832	Apr 26, 2021 (155)
48	GNOMAD	ss4066942833	Apr 26, 2021 (155)
49	GNOMAD	ss4066942834	Apr 26, 2021 (155)
50	GNOMAD	ss4066942835	Apr 26, 2021 (155)
51	GNOMAD	ss4066942836	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5158087166	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5158087167	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5158087168	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5158087169	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5158087170	Apr 26, 2021 (155)
57	1000G_HIGH_COVERAGE	ss5253270389	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5253270390	Oct 13, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5253270391	Oct 13, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5253270392	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5253270393	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5452745689	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5452745690	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5452745691	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5452745692	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5452745693	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5452745694	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5689437495	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5689437496	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5689437497	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5689437498	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5689437499	Oct 13, 2022 (156)
73	EVA	ss5825431671	Oct 13, 2022 (156)
74	EVA	ss5825431672	Oct 13, 2022 (156)
75	EVA	ss5825431673	Oct 13, 2022 (156)
76	EVA	ss5867888218	Oct 13, 2022 (156)
77	1000Genomes	NC_000003.11 - 20226419	Oct 12, 2018 (152)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7885038 (NC_000003.11:20226418:A: 884/3854) Row 7885039 (NC_000003.11:20226418::AAA 673/3854)	-	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7885038 (NC_000003.11:20226418:A: 884/3854) Row 7885039 (NC_000003.11:20226418::AAA 673/3854)	-	Oct 12, 2018 (152)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 100877073 (NC_000003.12:20184926::A 17870/137948) Row 100877074 (NC_000003.12:20184926::AA 1668/137980) Row 100877075 (NC_000003.12:20184926::AAA 17513/137852)...	-	Apr 26, 2021 (155)
86	Northern Sweden Submission ignored due to conflicting rows: Row 2971292 (NC_000003.11:20226418::AAA 81/596) Row 2971293 (NC_000003.11:20226418:A: 173/596) Row 2971294 (NC_000003.11:20226418::A 37/596)	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 2971292 (NC_000003.11:20226418::AAA 81/596) Row 2971293 (NC_000003.11:20226418:A: 173/596) Row 2971294 (NC_000003.11:20226418::A 37/596)	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 2971292 (NC_000003.11:20226418::AAA 81/596) Row 2971293 (NC_000003.11:20226418:A: 173/596) Row 2971294 (NC_000003.11:20226418::A 37/596)	-	Jul 13, 2019 (153)
89	8.3KJPN Submission ignored due to conflicting rows: Row 16056473 (NC_000003.11:20226418:A: 12529/16760) Row 16056474 (NC_000003.11:20226418::A 3830/16760) Row 16056475 (NC_000003.11:20226418::AAA 44/16760)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 16056473 (NC_000003.11:20226418:A: 12529/16760) Row 16056474 (NC_000003.11:20226418::A 3830/16760) Row 16056475 (NC_000003.11:20226418::AAA 44/16760)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 16056473 (NC_000003.11:20226418:A: 12529/16760) Row 16056474 (NC_000003.11:20226418::A 3830/16760) Row 16056475 (NC_000003.11:20226418::AAA 44/16760)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 16056473 (NC_000003.11:20226418:A: 12529/16760) Row 16056474 (NC_000003.11:20226418::A 3830/16760) Row 16056475 (NC_000003.11:20226418::AAA 44/16760)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 16056473 (NC_000003.11:20226418:A: 12529/16760) Row 16056474 (NC_000003.11:20226418::A 3830/16760) Row 16056475 (NC_000003.11:20226418::AAA 44/16760)...	-	Apr 26, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 23274599 (NC_000003.12:20184926:A: 21101/28258) Row 23274600 (NC_000003.12:20184926::A 6455/28258) Row 23274601 (NC_000003.12:20184926::AA 11/28258)...	-	Oct 13, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 23274599 (NC_000003.12:20184926:A: 21101/28258) Row 23274600 (NC_000003.12:20184926::A 6455/28258) Row 23274601 (NC_000003.12:20184926::AA 11/28258)...	-	Oct 13, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 23274599 (NC_000003.12:20184926:A: 21101/28258) Row 23274600 (NC_000003.12:20184926::A 6455/28258) Row 23274601 (NC_000003.12:20184926::AA 11/28258)...	-	Oct 13, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 23274599 (NC_000003.12:20184926:A: 21101/28258) Row 23274600 (NC_000003.12:20184926::A 6455/28258) Row 23274601 (NC_000003.12:20184926::AA 11/28258)...	-	Oct 13, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 23274599 (NC_000003.12:20184926:A: 21101/28258) Row 23274600 (NC_000003.12:20184926::A 6455/28258) Row 23274601 (NC_000003.12:20184926::AA 11/28258)...	-	Oct 13, 2022 (156)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7885038 (NC_000003.11:20226418:A: 861/3708) Row 7885039 (NC_000003.11:20226418::AAA 688/3708)	-	Oct 12, 2018 (152)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7885038 (NC_000003.11:20226418:A: 861/3708) Row 7885039 (NC_000003.11:20226418::AAA 688/3708)	-	Oct 12, 2018 (152)
101	ALFA	NC_000003.12 - 20184927	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)
rs75228122	May 11, 2012 (137)
rs144118363	May 04, 2012 (137)
rs376715694	May 13, 2013 (138)
rs141075651	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAA	(self)
ss5158087170	NC_000003.11:20226418:AA:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAA	(self)
ss5689437499	NC_000003.12:20184926:AA:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAA
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAA	(self)
ss80543279, ss81187864	NC_000003.9:20201431:A:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
ss288329852, ss295090657, ss326345767, ss326475152, ss551212877, ss551290194, ss553003666	NC_000003.10:20201422:A:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
ss663395867, ss1703536637, ss1703536638, ss1798956507, ss2991932370, ss3729686428, ss5158087166, ss5825431672	NC_000003.11:20226418:A:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
ss3645700172, ss3708764147, ss3802888044, ss4066942836, ss5253270389, ss5452745691, ss5689437495, ss5867888218	NC_000003.12:20184926:A:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
ss154749675	NT_022517.18:20166418:A:	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAA	(self)
ss326368211	NC_000003.10:20201422::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss288329854	NC_000003.10:20201432::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
14213538, ss1370058098, ss1798956504, ss3729686429, ss3827692183, ss5158087167, ss5825431673	NC_000003.11:20226418::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3802888046, ss4066942831, ss5253270391, ss5452745689, ss5689437496	NC_000003.12:20184926::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3708764146	NC_000003.12:20184927::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss287721447	NT_022517.18:20166428::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss193661176	NT_022517.19:20174926::A	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss5158087169	NC_000003.11:20226418::AA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4066942832, ss5253270392, ss5452745692, ss5689437497	NC_000003.12:20184926::AA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3708764145	NC_000003.12:20184927::AA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAA	(self)
14213538, ss666199133, ss1370058101, ss3729686427, ss3784251729, ss3789777640, ss3794651411, ss5158087168, ss5825431671	NC_000003.11:20226418::AAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710070102, ss1710070117, ss3745654195	NC_000003.11:20226419::AAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064899023, ss3802888045, ss4066942833, ss5253270390, ss5452745690, ss5689437498	NC_000003.12:20184926::AAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3708764144, ss3802888043	NC_000003.12:20184927::AAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3745654194	NC_000003.11:20226419::AAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4066942834, ss5253270393, ss5452745693	NC_000003.12:20184926::AAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3708764143	NC_000003.12:20184927::AAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4066942835, ss5452745694	NC_000003.12:20184926::AAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7738398846	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:20184926:AAAAAAAAAA:A… NC_000003.12:20184926:AAAAAAAAAA:AAAAAAAAAAAAAAA	(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 rs60350092

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs60350092