Name: rs35102693
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.

rs35102693

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:81679724-81679741 (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)₆ / del(A)₅ / del(A)₄ / delA…
del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.02686 (296/11020, ALFA)
delA=0.1911 (957/5008, 1000G)
delAA=0.1635 (630/3854, ALSPAC) (+ 2 more)
delAA=0.1694 (628/3708, TWINSUK)
delAA=0.016 (9/564, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	11020	AAAAAAAAAAAAAAAAAA=0.96125	AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.01189, AAAAAAAAAAAAAAAAA=0.02686, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.95	0.003358	0.046642	30
European	Sub	9056	AAAAAAAAAAAAAAAAAA=0.9528	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0145, AAAAAAAAAAAAAAAAA=0.0327, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.938785	0.004111	0.057104	22
African	Sub	1062	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	40	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1022	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	76	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	58	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	72	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	428	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	66	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	260	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=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	11020	(A)₁₈=0.96125	del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.01189, delA=0.02686, dupA=0.00000, dupAA=0.00000, dup(A)₅=0.00000
Allele Frequency Aggregator	European	Sub	9056	(A)₁₈=0.9528	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0145, delA=0.0327, dupA=0.0000, dupAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	1062	(A)₁₈=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	428	(A)₁₈=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	260	(A)₁₈=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Asian	Sub	76	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	72	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	66	(A)₁₈=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₅=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₈=0.8089	delA=0.1911
1000Genomes	African	Sub	1322	(A)₁₈=0.7496	delA=0.2504
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.9107	delA=0.0893
1000Genomes	Europe	Sub	1006	(A)₁₈=0.7664	delA=0.2336
1000Genomes	South Asian	Sub	978	(A)₁₈=0.881	delA=0.119
1000Genomes	American	Sub	694	(A)₁₈=0.733	delA=0.267
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₈=0.8365	delAA=0.1635
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₈=0.8306	delAA=0.1694
Northern Sweden	ACPOP	Study-wide	564	(A)₁₈=0.984	delAA=0.016

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.81679736_81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679737_81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679738_81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679739_81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679740_81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679741del
GRCh38.p14 chr 17	NC_000017.11:g.81679741dup
GRCh38.p14 chr 17	NC_000017.11:g.81679740_81679741dup
GRCh38.p14 chr 17	NC_000017.11:g.81679737_81679741dup
GRCh37.p13 chr 17	NC_000017.10:g.79646766_79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646767_79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646768_79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646769_79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646770_79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646771del
GRCh37.p13 chr 17	NC_000017.10:g.79646771dup
GRCh37.p13 chr 17	NC_000017.10:g.79646770_79646771dup
GRCh37.p13 chr 17	NC_000017.10:g.79646767_79646771dup
ARL16 RefSeqGene	NG_051248.1:g.9196_9201del
ARL16 RefSeqGene	NG_051248.1:g.9197_9201del
ARL16 RefSeqGene	NG_051248.1:g.9198_9201del
ARL16 RefSeqGene	NG_051248.1:g.9199_9201del
ARL16 RefSeqGene	NG_051248.1:g.9200_9201del
ARL16 RefSeqGene	NG_051248.1:g.9201del
ARL16 RefSeqGene	NG_051248.1:g.9201dup
ARL16 RefSeqGene	NG_051248.1:g.9200_9201dup
ARL16 RefSeqGene	NG_051248.1:g.9197_9201dup

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₈=	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₅
GRCh38.p14 chr 17	NC_000017.11:g.81679724_81679741=	NC_000017.11:g.81679736_81679741del	NC_000017.11:g.81679737_81679741del	NC_000017.11:g.81679738_81679741del	NC_000017.11:g.81679739_81679741del	NC_000017.11:g.81679740_81679741del	NC_000017.11:g.81679741del	NC_000017.11:g.81679741dup	NC_000017.11:g.81679740_81679741dup	NC_000017.11:g.81679737_81679741dup
GRCh37.p13 chr 17	NC_000017.10:g.79646754_79646771=	NC_000017.10:g.79646766_79646771del	NC_000017.10:g.79646767_79646771del	NC_000017.10:g.79646768_79646771del	NC_000017.10:g.79646769_79646771del	NC_000017.10:g.79646770_79646771del	NC_000017.10:g.79646771del	NC_000017.10:g.79646771dup	NC_000017.10:g.79646770_79646771dup	NC_000017.10:g.79646767_79646771dup
ARL16 RefSeqGene	NG_051248.1:g.9184_9201=	NG_051248.1:g.9196_9201del	NG_051248.1:g.9197_9201del	NG_051248.1:g.9198_9201del	NG_051248.1:g.9199_9201del	NG_051248.1:g.9200_9201del	NG_051248.1:g.9201del	NG_051248.1:g.9201dup	NG_051248.1:g.9200_9201dup	NG_051248.1:g.9197_9201dup

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#.

42 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40754165	Mar 15, 2016 (147)
2	HUMANGENOME_JCVI	ss96571780	Mar 15, 2016 (147)
3	GMI	ss289341543	May 04, 2012 (137)
4	SSMP	ss664380927	Apr 01, 2015 (144)
5	1000GENOMES	ss1377058847	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1708870340	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1708870420	Apr 01, 2015 (144)
8	SWEGEN	ss3015996480	Nov 08, 2017 (151)
9	MCHAISSO	ss3063880016	Nov 08, 2017 (151)
10	EVA_DECODE	ss3701031037	Jul 13, 2019 (153)
11	EVA_DECODE	ss3701031038	Jul 13, 2019 (153)
12	EVA_DECODE	ss3701031039	Jul 13, 2019 (153)
13	EVA_DECODE	ss3701031040	Jul 13, 2019 (153)
14	ACPOP	ss3742266596	Jul 13, 2019 (153)
15	PACBIO	ss3788283633	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3820266789	Jul 13, 2019 (153)
17	EVA	ss3835007878	Apr 27, 2020 (154)
18	GNOMAD	ss4316606991	Apr 26, 2021 (155)
19	GNOMAD	ss4316606992	Apr 26, 2021 (155)
20	GNOMAD	ss4316606993	Apr 26, 2021 (155)
21	GNOMAD	ss4316606994	Apr 26, 2021 (155)
22	GNOMAD	ss4316606995	Apr 26, 2021 (155)
23	GNOMAD	ss4316606996	Apr 26, 2021 (155)
24	GNOMAD	ss4316606997	Apr 26, 2021 (155)
25	GNOMAD	ss4316606998	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5223737852	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5223737853	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5223737854	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5223737855	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5304136680	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5304136682	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5304136683	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5304136684	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5497080573	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5497080574	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5497080576	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5780374617	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5780374618	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5780374619	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5780374621	Oct 16, 2022 (156)
41	EVA	ss5851922061	Oct 16, 2022 (156)
42	EVA	ss5952056119	Oct 16, 2022 (156)
43	1000Genomes	NC_000017.10 - 79646754	Oct 12, 2018 (152)
44	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 79646754	Oct 12, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 515416868 (NC_000017.11:81679723::A 295/80076) Row 515416869 (NC_000017.11:81679723::AA 4/80272) Row 515416870 (NC_000017.11:81679723::AAAAA 1/80278)...	-	Apr 26, 2021 (155)
53	Northern Sweden	NC_000017.10 - 79646754	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 81707159 (NC_000017.10:79646753:A: 197/16642) Row 81707160 (NC_000017.10:79646753:AA: 4168/16642) Row 81707161 (NC_000017.10:79646753::A 16/16642)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 81707159 (NC_000017.10:79646753:A: 197/16642) Row 81707160 (NC_000017.10:79646753:AA: 4168/16642) Row 81707161 (NC_000017.10:79646753::A 16/16642)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 81707159 (NC_000017.10:79646753:A: 197/16642) Row 81707160 (NC_000017.10:79646753:AA: 4168/16642) Row 81707161 (NC_000017.10:79646753::A 16/16642)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 81707159 (NC_000017.10:79646753:A: 197/16642) Row 81707160 (NC_000017.10:79646753:AA: 4168/16642) Row 81707161 (NC_000017.10:79646753::A 16/16642)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 114211721 (NC_000017.11:81679723:AA: 7760/28242) Row 114211722 (NC_000017.11:81679723:A: 368/28242) Row 114211723 (NC_000017.11:81679723::A 33/28242)...	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 114211721 (NC_000017.11:81679723:AA: 7760/28242) Row 114211722 (NC_000017.11:81679723:A: 368/28242) Row 114211723 (NC_000017.11:81679723::A 33/28242)...	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 114211721 (NC_000017.11:81679723:AA: 7760/28242) Row 114211722 (NC_000017.11:81679723:A: 368/28242) Row 114211723 (NC_000017.11:81679723::A 33/28242)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 114211721 (NC_000017.11:81679723:AA: 7760/28242) Row 114211722 (NC_000017.11:81679723:A: 368/28242) Row 114211723 (NC_000017.11:81679723::A 33/28242)...	-	Oct 16, 2022 (156)
62	UK 10K study - Twins	NC_000017.10 - 79646754	Oct 12, 2018 (152)
63	ALFA	NC_000017.11 - 81679724	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)
rs66710238	May 11, 2012 (137)
rs66710239	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5223737855	NC_000017.10:79646753:AAAAAA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5780374621	NC_000017.11:81679723:AAAAAA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA
ss4316606998	NC_000017.11:81679723:AAAAA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4316606997	NC_000017.11:81679723:AAAA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3701031040, ss4316606996, ss5304136684	NC_000017.11:81679723:AAA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
40475001, 15551461, 40475001, ss664380927, ss1708870340, ss1708870420, ss3015996480, ss3742266596, ss3835007878, ss5223737853, ss5952056119	NC_000017.10:79646753:AA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3063880016, ss4316606995, ss5304136680, ss5497080574, ss5780374617, ss5851922061	NC_000017.11:81679723:AA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3701031039	NC_000017.11:81679724:AA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss96571780	NT_010783.15:44920905:AA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40754165	NT_010783.15:44920921:AA:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss289341543	NC_000017.9:77257158:A:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
73044958, ss1377058847, ss3788283633, ss5223737852	NC_000017.10:79646753:A:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3820266789, ss4316606994, ss5304136682, ss5497080573, ss5780374618	NC_000017.11:81679723:A:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3701031038	NC_000017.11:81679725:A:	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5223737854	NC_000017.10:79646753::A	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4316606991, ss5304136683, ss5497080576, ss5780374619	NC_000017.11:81679723::A	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3701031037	NC_000017.11:81679726::A	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4316606992	NC_000017.11:81679723::AA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4316606993	NC_000017.11:81679723::AAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12364704879	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:81679723:AAAAAAAAAAAA… NC_000017.11:81679723:AAAAAAAAAAAAAAAAAA: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 rs35102693

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

rs35102693