Name: rs373010361
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.

rs373010361

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:46974734-46974749 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/9246, ALFA)
delA=0.0000 (0/9246, ALFA)
dupA=0.0000 (0/9246, ALFA) (+ 2 more)
delA=0.1050 (176/1676, Korea1K)
delA=0.05 (2/40, GENOME_DK)

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	9246	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	6122	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1988	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	72	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1916	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	84	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	66	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	18	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	122	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	516	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	62	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	352	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	9246	(A)₁₆=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	European	Sub	6122	(A)₁₆=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	African	Sub	1988	(A)₁₆=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	516	(A)₁₆=1.000	delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	352	(A)₁₆=1.000	delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	122	(A)₁₆=1.000	delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Asian	Sub	84	(A)₁₆=1.00	delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(A)₁₆=1.00	delAA=0.00, delA=0.00, dupA=0.00
Korean Genome Project	KOREAN	Study-wide	1676	(A)₁₆=0.8950	delA=0.1050
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₆=0.95	delA=0.05

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.46974746_46974749del
GRCh38.p14 chr 17	NC_000017.11:g.46974747_46974749del
GRCh38.p14 chr 17	NC_000017.11:g.46974748_46974749del
GRCh38.p14 chr 17	NC_000017.11:g.46974749del
GRCh38.p14 chr 17	NC_000017.11:g.46974749dup
GRCh38.p14 chr 17	NC_000017.11:g.46974748_46974749dup
GRCh38.p14 chr 17	NC_000017.11:g.46974743_46974749dup
GRCh37.p13 chr 17	NC_000017.10:g.45052112_45052115del
GRCh37.p13 chr 17	NC_000017.10:g.45052113_45052115del
GRCh37.p13 chr 17	NC_000017.10:g.45052114_45052115del
GRCh37.p13 chr 17	NC_000017.10:g.45052115del
GRCh37.p13 chr 17	NC_000017.10:g.45052115dup
GRCh37.p13 chr 17	NC_000017.10:g.45052114_45052115dup
GRCh37.p13 chr 17	NC_000017.10:g.45052109_45052115dup

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.4810-743… XM_024450773.2:c.4810-74310_4810-74307del	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

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

Molecule type	Change	Amino acid[Codon]	SO Term
GOSR2 transcript variant C	NM_001012511.3:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant D	NM_001321133.2: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	Genic Downstream Transcript Variant
GOSR2 transcript variant K	NR_148350.2:n.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant L	NR_148351.2:n.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X3	XM_017025383.3:c.677-453_… XM_017025383.3:c.677-453_677-450del	N/A	Intron Variant
GOSR2 transcript variant X4	XM_006722190.5:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X8	XM_011525501.4:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X9	XM_011525502.4:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X1	XM_017025378.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X5	XM_017025386.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X6	XM_017025387.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X21	XM_017025389.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X10	XM_017025392.2:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X12	XM_047437112.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X15	XM_047437113.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X16	XM_047437114.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X17	XM_047437115.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X2	XM_047437116.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X18	XM_047437117.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X19	XM_047437118.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X7	XM_047437119.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X11	XM_047437120.1:c.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X13	XR_007065552.1:n.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X14	XR_007065553.1:n.	N/A	Genic Downstream Transcript Variant
GOSR2 transcript variant X20	XR_934616.4: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)₁₆=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₇
GRCh38.p14 chr 17	NC_000017.11:g.46974734_46974749=	NC_000017.11:g.46974746_46974749del	NC_000017.11:g.46974747_46974749del	NC_000017.11:g.46974748_46974749del	NC_000017.11:g.46974749del	NC_000017.11:g.46974749dup	NC_000017.11:g.46974748_46974749dup	NC_000017.11:g.46974743_46974749dup
GRCh37.p13 chr 17	NC_000017.10:g.45052100_45052115=	NC_000017.10:g.45052112_45052115del	NC_000017.10:g.45052113_45052115del	NC_000017.10:g.45052114_45052115del	NC_000017.10:g.45052115del	NC_000017.10:g.45052115dup	NC_000017.10:g.45052114_45052115dup	NC_000017.10:g.45052109_45052115dup
GOSR2 transcript variant X3	XM_017025383.3:c.677-465=	XM_017025383.3:c.677-453_677-450del	XM_017025383.3:c.677-452_677-450del	XM_017025383.3:c.677-451_677-450del	XM_017025383.3:c.677-450del	XM_017025383.3:c.677-450dup	XM_017025383.3:c.677-451_677-450dup	XM_017025383.3:c.677-456_677-450dup
LRRC37A2 transcript variant X16	XM_024450773.2:c.4810-74322=	XM_024450773.2:c.4810-74310_4810-74307del	XM_024450773.2:c.4810-74309_4810-74307del	XM_024450773.2:c.4810-74308_4810-74307del	XM_024450773.2:c.4810-74307del	XM_024450773.2:c.4810-74307dup	XM_024450773.2:c.4810-74308_4810-74307dup	XM_024450773.2:c.4810-74313_4810-74307dup

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#.

37 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4279662	Mar 15, 2016 (147)
2	TSC-CSHL	ss4303939	Mar 15, 2016 (147)
3	BILGI_BIOE	ss666692591	Apr 25, 2013 (138)
4	EVA_GENOME_DK	ss1575054465	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1708769841	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1708769892	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710732778	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710732781	Apr 01, 2015 (144)
9	HAMMER_LAB	ss1808795661	Sep 08, 2015 (146)
10	SYSTEMSBIOZJU	ss2629032703	Nov 08, 2017 (151)
11	MCHAISSO	ss3065652013	Nov 08, 2017 (151)
12	EVA_DECODE	ss3700524503	Jul 13, 2019 (153)
13	EVA_DECODE	ss3700524504	Jul 13, 2019 (153)
14	EVA_DECODE	ss3700524505	Jul 13, 2019 (153)
15	EVA_DECODE	ss3700524506	Jul 13, 2019 (153)
16	EVA_DECODE	ss3700524507	Jul 13, 2019 (153)
17	EVA	ss3834882526	Apr 27, 2020 (154)
18	EVA	ss3841052786	Apr 27, 2020 (154)
19	EVA	ss3846549698	Apr 27, 2020 (154)
20	KOGIC	ss3978892383	Apr 27, 2020 (154)
21	GNOMAD	ss4312134629	Apr 27, 2021 (155)
22	GNOMAD	ss4312134630	Apr 27, 2021 (155)
23	GNOMAD	ss4312134631	Apr 27, 2021 (155)
24	GNOMAD	ss4312134632	Apr 27, 2021 (155)
25	GNOMAD	ss4312134633	Apr 27, 2021 (155)
26	TOMMO_GENOMICS	ss5222564311	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5222564312	Apr 27, 2021 (155)
28	HUGCELL_USP	ss5496275830	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5496275831	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5778822537	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5778822538	Oct 16, 2022 (156)
32	YY_MCH	ss5816565017	Oct 16, 2022 (156)
33	EVA	ss5834024569	Oct 16, 2022 (156)
34	EVA	ss5834024570	Oct 16, 2022 (156)
35	EVA	ss5834024571	Oct 16, 2022 (156)
36	EVA	ss5851817316	Oct 16, 2022 (156)
37	EVA	ss5980969780	Oct 16, 2022 (156)
38	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39906398 (NC_000017.10:45052099:A: 1381/3854) Row 39906399 (NC_000017.10:45052099::AA 976/3854)	-	Oct 12, 2018 (152)
39	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39906398 (NC_000017.10:45052099:A: 1381/3854) Row 39906399 (NC_000017.10:45052099::AA 976/3854)	-	Oct 12, 2018 (152)
40	The Danish reference pan genome	NC_000017.10 - 45052100	Apr 27, 2020 (154)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508112180 (NC_000017.11:46974733::A 23/59166) Row 508112181 (NC_000017.11:46974733:A: 14880/59080) Row 508112182 (NC_000017.11:46974733:AA: 697/59158)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508112180 (NC_000017.11:46974733::A 23/59166) Row 508112181 (NC_000017.11:46974733:A: 14880/59080) Row 508112182 (NC_000017.11:46974733:AA: 697/59158)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508112180 (NC_000017.11:46974733::A 23/59166) Row 508112181 (NC_000017.11:46974733:A: 14880/59080) Row 508112182 (NC_000017.11:46974733:AA: 697/59158)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508112180 (NC_000017.11:46974733::A 23/59166) Row 508112181 (NC_000017.11:46974733:A: 14880/59080) Row 508112182 (NC_000017.11:46974733:AA: 697/59158)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508112180 (NC_000017.11:46974733::A 23/59166) Row 508112181 (NC_000017.11:46974733:A: 14880/59080) Row 508112182 (NC_000017.11:46974733:AA: 697/59158)...	-	Apr 27, 2021 (155)
46	Korean Genome Project	NC_000017.11 - 46974734	Apr 27, 2020 (154)
47	8.3KJPN Submission ignored due to conflicting rows: Row 80533618 (NC_000017.10:45052099:A: 1278/15902) Row 80533619 (NC_000017.10:45052099::A 1/15902)	-	Apr 27, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 80533618 (NC_000017.10:45052099:A: 1278/15902) Row 80533619 (NC_000017.10:45052099::A 1/15902)	-	Apr 27, 2021 (155)
49	14KJPN Submission ignored due to conflicting rows: Row 112659641 (NC_000017.11:46974733:A: 2250/28256) Row 112659642 (NC_000017.11:46974733::A 1/28256)	-	Oct 16, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 112659641 (NC_000017.11:46974733:A: 2250/28256) Row 112659642 (NC_000017.11:46974733::A 1/28256)	-	Oct 16, 2022 (156)
51	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39906398 (NC_000017.10:45052099:A: 1287/3708) Row 39906399 (NC_000017.10:45052099::AA 893/3708)	-	Oct 12, 2018 (152)
52	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39906398 (NC_000017.10:45052099:A: 1287/3708) Row 39906399 (NC_000017.10:45052099::AA 893/3708)	-	Oct 12, 2018 (152)
53	ALFA	NC_000017.11 - 46974734	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)
rs3072549	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4312134633	NC_000017.11:46974733:AAAA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5980969780	NC_000017.10:45052099:AAA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA
ss3700524507, ss4312134632	NC_000017.11:46974733:AAA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5834024569	NC_000017.10:45052099:AA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA
ss4312134631, ss5496275831	NC_000017.11:46974733:AA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7991529478	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3700524506	NC_000017.11:46974734:AA:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
563569, ss666692591, ss1575054465, ss1708769841, ss1708769892, ss1808795661, ss2629032703, ss3834882526, ss3841052786, ss5222564311, ss5834024571	NC_000017.10:45052099:A:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
35270384, ss3065652013, ss3846549698, ss3978892383, ss4312134630, ss5496275830, ss5778822537, ss5816565017, ss5851817316	NC_000017.11:46974733:A:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7991529478	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3700524505	NC_000017.11:46974735:A:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4303939	NT_010783.15:10326253:A:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4279662	NT_010783.15:10326266:A:	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5222564312	NC_000017.10:45052099::A	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4312134629, ss5778822538	NC_000017.11:46974733::A	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7991529478	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4303939	NT_010783.15:10326253:A:AA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4279662	NT_010783.15:10326266:A:AA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5834024570	NC_000017.10:45052099::AA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss1710732778, ss1710732781	NC_000017.10:45052100::AA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3700524504	NC_000017.11:46974736::AA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3700524503	NC_000017.11:46974736::AAAAAAA	NC_000017.11:46974733:AAAAAAAAAAAA… NC_000017.11:46974733:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(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 rs373010361

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

rs373010361