Name: rs661665
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.

rs661665

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:21042269 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.458189 (121278/264690, TOPMED)
C=0.08196 (2316/28258, 14KJPN)
A=0.43326 (9802/22624, ALFA) (+ 17 more)
C=0.08311 (1393/16760, 8.3KJPN)
C=0.4491 (2876/6404, 1000G_30x)
C=0.4367 (2187/5008, 1000G)
C=0.4317 (1934/4480, Estonian)
C=0.4990 (1923/3854, ALSPAC)
A=0.4919 (1824/3708, TWINSUK)
C=0.1175 (344/2928, KOREAN)
C=0.1141 (209/1832, Korea1K)
A=0.4094 (461/1126, PharmGKB)
C=0.468 (467/998, GoNL)
A=0.498 (299/600, NorthernSweden)
A=0.494 (264/534, MGP)
C=0.221 (107/484, SGDP_PRJ)
C=0.426 (92/216, Qatari)
C=0.187 (40/214, Vietnamese)
C=0.26 (12/46, Siberian)
A=0.42 (17/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: APOB : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	22624	C=0.56674	A=0.43326, T=0.00000
European	Sub	18998	C=0.53021	A=0.46979, T=0.00000
African	Sub	1810	C=0.9541	A=0.0459, T=0.0000
African Others	Sub	74	C=0.91	A=0.09, T=0.00
African American	Sub	1736	C=0.9562	A=0.0438, T=0.0000
Asian	Sub	20	C=0.15	A=0.85, T=0.00
East Asian	Sub	16	C=0.19	A=0.81, T=0.00
Other Asian	Sub	4	C=0.0	A=1.0, T=0.0
Latin American 1	Sub	56	C=0.80	A=0.20, T=0.00
Latin American 2	Sub	200	C=0.685	A=0.315, T=0.000
South Asian	Sub	36	C=0.69	A=0.31, T=0.00
Other	Sub	1504	C=0.5399	A=0.4601, T=0.0000

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
TopMed	Global	Study-wide	264690	C=0.541811	A=0.458189
14KJPN	JAPANESE	Study-wide	28258	C=0.08196	A=0.91804
Allele Frequency Aggregator	Total	Global	22624	C=0.56674	A=0.43326, T=0.00000
Allele Frequency Aggregator	European	Sub	18998	C=0.53021	A=0.46979, T=0.00000
Allele Frequency Aggregator	African	Sub	1810	C=0.9541	A=0.0459, T=0.0000
Allele Frequency Aggregator	Other	Sub	1504	C=0.5399	A=0.4601, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	200	C=0.685	A=0.315, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	56	C=0.80	A=0.20, T=0.00
Allele Frequency Aggregator	South Asian	Sub	36	C=0.69	A=0.31, T=0.00
Allele Frequency Aggregator	Asian	Sub	20	C=0.15	A=0.85, T=0.00
8.3KJPN	JAPANESE	Study-wide	16760	C=0.08311	A=0.91689
1000Genomes_30x	Global	Study-wide	6404	C=0.4491	A=0.5509
1000Genomes_30x	African	Sub	1786	C=0.7374	A=0.2626
1000Genomes_30x	Europe	Sub	1266	C=0.5103	A=0.4897
1000Genomes_30x	South Asian	Sub	1202	C=0.2646	A=0.7354
1000Genomes_30x	East Asian	Sub	1170	C=0.1282	A=0.8718
1000Genomes_30x	American	Sub	980	C=0.454	A=0.546
1000Genomes	Global	Study-wide	5008	C=0.4367	A=0.5633
1000Genomes	African	Sub	1322	C=0.7322	A=0.2678
1000Genomes	East Asian	Sub	1008	C=0.1210	A=0.8790
1000Genomes	Europe	Sub	1006	C=0.5080	A=0.4920
1000Genomes	South Asian	Sub	978	C=0.268	A=0.732
1000Genomes	American	Sub	694	C=0.467	A=0.533
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.4317	A=0.5683
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.4990	A=0.5010
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.5081	A=0.4919
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.1175	A=0.8825, G=0.0000, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	C=0.1141	A=0.8859
PharmGKB Aggregated	Global	Study-wide	1126	C=0.5906	A=0.4094
PharmGKB Aggregated	PA141161503	Sub	946	C=0.566	A=0.434
PharmGKB Aggregated	PA128749333	Sub	94	C=0.73	A=0.27
PharmGKB Aggregated	PA151853697	Sub	86	C=0.71	A=0.29
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.468	A=0.532
Northern Sweden	ACPOP	Study-wide	600	C=0.502	A=0.498
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	C=0.506	A=0.494
SGDP_PRJ	Global	Study-wide	484	C=0.221	A=0.779
Qatari	Global	Study-wide	216	C=0.426	A=0.574
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.187	A=0.813
Siberian	Global	Study-wide	46	C=0.26	A=0.74
The Danish reference pan genome	Danish	Study-wide	40	C=0.57	A=0.42

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 2	NC_000002.12:g.21042269C>A
GRCh38.p14 chr 2	NC_000002.12:g.21042269C>G
GRCh38.p14 chr 2	NC_000002.12:g.21042269C>T
GRCh37.p13 chr 2	NC_000002.11:g.21265141C>A
GRCh37.p13 chr 2	NC_000002.11:g.21265141C>G
GRCh37.p13 chr 2	NC_000002.11:g.21265141C>T
LOC106560211 genomic region	NG_042873.1:g.1282C>A
LOC106560211 genomic region	NG_042873.1:g.1282C>G
LOC106560211 genomic region	NG_042873.1:g.1282C>T
APOB RefSeqGene	NG_011793.1:g.6805G>T
APOB RefSeqGene	NG_011793.1:g.6805G>C
APOB RefSeqGene	NG_011793.1:g.6805G>A
GRCh38.p14 chr 2 fix patch HG2231_HG2496_PATCH	NW_025791767.1:g.92937C>A
GRCh38.p14 chr 2 fix patch HG2231_HG2496_PATCH	NW_025791767.1:g.92937C>G
GRCh38.p14 chr 2 fix patch HG2231_HG2496_PATCH	NW_025791767.1:g.92937C>T

Gene: APOB, apolipoprotein B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
APOB transcript	NM_000384.3:c.237+92G>T	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.

Allele: A (allele ID: 1182349 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001553837.2	Hypercholesterolemia, autosomal dominant, type B	Benign
RCV001553838.2	Familial hypobetalipoproteinemia 1	Benign

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	C=	A	G	T
GRCh38.p14 chr 2	NC_000002.12:g.21042269=	NC_000002.12:g.21042269C>A	NC_000002.12:g.21042269C>G	NC_000002.12:g.21042269C>T
GRCh37.p13 chr 2	NC_000002.11:g.21265141=	NC_000002.11:g.21265141C>A	NC_000002.11:g.21265141C>G	NC_000002.11:g.21265141C>T
LOC106560211 genomic region	NG_042873.1:g.1282=	NG_042873.1:g.1282C>A	NG_042873.1:g.1282C>G	NG_042873.1:g.1282C>T
APOB RefSeqGene	NG_011793.1:g.6805=	NG_011793.1:g.6805G>T	NG_011793.1:g.6805G>C	NG_011793.1:g.6805G>A
GRCh38.p14 chr 2 fix patch HG2231_HG2496_PATCH	NW_025791767.1:g.92937=	NW_025791767.1:g.92937C>A	NW_025791767.1:g.92937C>G	NW_025791767.1:g.92937C>T
APOB transcript	NM_000384.2:c.237+92=	NM_000384.2:c.237+92G>T	NM_000384.2:c.237+92G>C	NM_000384.2:c.237+92G>A
APOB transcript	NM_000384.3:c.237+92=	NM_000384.3:c.237+92G>T	NM_000384.3:c.237+92G>C	NM_000384.3:c.237+92G>A

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#.

99 SubSNP, 22 Frequency, 2 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss834852	Aug 11, 2000 (83)
2	WI_SSAHASNP	ss6424608	Feb 20, 2003 (111)
3	SSAHASNP	ss21641784	Apr 05, 2004 (121)
4	IMCJ-GDT	ss22886737	Apr 05, 2004 (121)
5	PARC	ss23143745	Sep 20, 2004 (126)
6	ABI	ss44351757	Mar 11, 2006 (126)
7	PHARMGKB_PARC	ss69365767	May 17, 2007 (127)
8	PHARMGKB_PARC	ss69369339	May 17, 2007 (127)
9	PHARMGKB_PARC	ss84143811	Dec 14, 2007 (130)
10	BCMHGSC_JDW	ss91083058	Mar 24, 2008 (129)
11	BGI	ss106074460	Feb 04, 2009 (130)
12	1000GENOMES	ss109290561	Jan 23, 2009 (130)
13	1000GENOMES	ss109938336	Jan 24, 2009 (130)
14	ENSEMBL	ss135984509	Dec 01, 2009 (131)
15	ENSEMBL	ss138402922	Dec 01, 2009 (131)
16	GMI	ss156788156	Dec 01, 2009 (131)
17	COMPLETE_GENOMICS	ss163180392	Jul 04, 2010 (132)
18	BUSHMAN	ss200138536	Jul 04, 2010 (132)
19	1000GENOMES	ss219112811	Jul 14, 2010 (132)
20	1000GENOMES	ss231070873	Jul 14, 2010 (132)
21	1000GENOMES	ss238648611	Jul 15, 2010 (132)
22	ILLUMINA	ss244305693	Jul 04, 2010 (132)
23	BL	ss252965395	May 09, 2011 (134)
24	GMI	ss276380995	May 04, 2012 (137)
25	PJP	ss292525086	May 09, 2011 (134)
26	ILLUMINA	ss410831627	Sep 17, 2011 (135)
27	ILLUMINA	ss484003850	May 04, 2012 (137)
28	ILLUMINA	ss484332152	May 04, 2012 (137)
29	ILLUMINA	ss536515345	Sep 08, 2015 (146)
30	TISHKOFF	ss555407878	Apr 25, 2013 (138)
31	SSMP	ss648986525	Apr 25, 2013 (138)
32	ILLUMINA	ss780613886	Sep 08, 2015 (146)
33	ILLUMINA	ss782612303	Sep 08, 2015 (146)
34	ILLUMINA	ss836107323	Sep 08, 2015 (146)
35	EVA-GONL	ss976571014	Aug 21, 2014 (142)
36	JMKIDD_LAB	ss1068922844	Aug 21, 2014 (142)
37	1000GENOMES	ss1296219074	Aug 21, 2014 (142)
38	DDI	ss1428503024	Apr 01, 2015 (144)
39	EVA_GENOME_DK	ss1578774065	Apr 01, 2015 (144)
40	EVA_DECODE	ss1585973035	Apr 01, 2015 (144)
41	EVA_UK10K_ALSPAC	ss1602976122	Apr 01, 2015 (144)
42	EVA_UK10K_TWINSUK	ss1645970155	Apr 01, 2015 (144)
43	EVA_MGP	ss1710955744	Apr 01, 2015 (144)
44	HAMMER_LAB	ss1796398899	Sep 08, 2015 (146)
45	WEILL_CORNELL_DGM	ss1919804752	Feb 12, 2016 (147)
46	GENOMED	ss1968713783	Jul 19, 2016 (147)
47	JJLAB	ss2020429562	Sep 14, 2016 (149)
48	ILLUMINA	ss2094805669	Dec 20, 2016 (150)
49	ILLUMINA	ss2095088397	Dec 20, 2016 (150)
50	USC_VALOUEV	ss2148474120	Dec 20, 2016 (150)
51	HUMAN_LONGEVITY	ss2228150532	Dec 20, 2016 (150)
52	SYSTEMSBIOZJU	ss2624731663	Nov 08, 2017 (151)
53	ILLUMINA	ss2633582651	Nov 08, 2017 (151)
54	GRF	ss2703034121	Nov 08, 2017 (151)
55	GNOMAD	ss2770590086	Nov 08, 2017 (151)
56	SWEGEN	ss2989102328	Nov 08, 2017 (151)
57	BIOINF_KMB_FNS_UNIBA	ss3023982342	Nov 08, 2017 (151)
58	CSHL	ss3344112486	Nov 08, 2017 (151)
59	ILLUMINA	ss3628009368	Oct 11, 2018 (152)
60	ILLUMINA	ss3631551433	Oct 11, 2018 (152)
61	ILLUMINA	ss3642081321	Oct 11, 2018 (152)
62	OMUKHERJEE_ADBS	ss3646258669	Oct 11, 2018 (152)
63	URBANLAB	ss3646982749	Oct 11, 2018 (152)
64	ILLUMINA	ss3652376896	Oct 11, 2018 (152)
65	EGCUT_WGS	ss3657054906	Jul 12, 2019 (153)
66	EVA_DECODE	ss3703404063	Jul 12, 2019 (153)
67	ACPOP	ss3728221305	Jul 12, 2019 (153)
68	EVA	ss3756451880	Jul 12, 2019 (153)
69	PACBIO	ss3783799995	Jul 12, 2019 (153)
70	PACBIO	ss3789398118	Jul 12, 2019 (153)
71	PACBIO	ss3794270866	Jul 12, 2019 (153)
72	KHV_HUMAN_GENOMES	ss3800835695	Jul 12, 2019 (153)
73	EVA	ss3826860052	Apr 25, 2020 (154)
74	EVA	ss3836836543	Apr 25, 2020 (154)
75	EVA	ss3842250884	Apr 25, 2020 (154)
76	SGDP_PRJ	ss3851756329	Apr 25, 2020 (154)
77	KRGDB	ss3897153146	Apr 25, 2020 (154)
78	KOGIC	ss3947262000	Apr 25, 2020 (154)
79	FSA-LAB	ss3984169922	Apr 26, 2021 (155)
80	TOPMED	ss4496804738	Apr 26, 2021 (155)
81	TOMMO_GENOMICS	ss5150214051	Apr 26, 2021 (155)
82	1000G_HIGH_COVERAGE	ss5247184171	Oct 12, 2022 (156)
83	EVA	ss5314716540	Oct 12, 2022 (156)
84	EVA	ss5327303533	Oct 12, 2022 (156)
85	HUGCELL_USP	ss5447469719	Oct 12, 2022 (156)
86	EVA	ss5506320633	Oct 12, 2022 (156)
87	1000G_HIGH_COVERAGE	ss5521944174	Oct 12, 2022 (156)
88	EVA	ss5623919827	Oct 12, 2022 (156)
89	SANFORD_IMAGENETICS	ss5628249052	Oct 12, 2022 (156)
90	TOMMO_GENOMICS	ss5678502264	Oct 12, 2022 (156)
91	EVA	ss5800048223	Oct 12, 2022 (156)
92	EVA	ss5800092964	Oct 12, 2022 (156)
93	YY_MCH	ss5801993926	Oct 12, 2022 (156)
94	EVA	ss5819763751	Oct 12, 2022 (156)
95	EVA	ss5852422432	Oct 12, 2022 (156)
96	EVA	ss5929340482	Oct 12, 2022 (156)
97	EVA	ss5954446895	Oct 12, 2022 (156)
98	EVA	ss5980041736	Oct 12, 2022 (156)
99	EVA	ss5981203323	Oct 12, 2022 (156)
100	1000Genomes	NC_000002.11 - 21265141	Oct 11, 2018 (152)
101	1000Genomes_30x	NC_000002.12 - 21042269	Oct 12, 2022 (156)
102	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 21265141	Oct 11, 2018 (152)
103	Genetic variation in the Estonian population	NC_000002.11 - 21265141	Oct 11, 2018 (152)
104	The Danish reference pan genome	NC_000002.11 - 21265141	Apr 25, 2020 (154)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 50656896 (NC_000002.12:21042268:C:A 63963/140004) Row 50656897 (NC_000002.12:21042268:C:T 2/140070)	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 50656896 (NC_000002.12:21042268:C:A 63963/140004) Row 50656897 (NC_000002.12:21042268:C:T 2/140070)	-	Apr 26, 2021 (155)
107	Genome of the Netherlands Release 5	NC_000002.11 - 21265141	Apr 25, 2020 (154)
108	KOREAN population from KRGDB	NC_000002.11 - 21265141	Apr 25, 2020 (154)
109	Korean Genome Project	NC_000002.12 - 21042269	Apr 25, 2020 (154)
110	Medical Genome Project healthy controls from Spanish population	NC_000002.11 - 21265141	Apr 25, 2020 (154)
111	Northern Sweden	NC_000002.11 - 21265141	Jul 12, 2019 (153)
112	PharmGKB Aggregated	NC_000002.12 - 21042269	Apr 25, 2020 (154)
113	Qatari	NC_000002.11 - 21265141	Apr 25, 2020 (154)
114	SGDP_PRJ	NC_000002.11 - 21265141	Apr 25, 2020 (154)
115	Siberian	NC_000002.11 - 21265141	Apr 25, 2020 (154)
116	8.3KJPN	NC_000002.11 - 21265141	Apr 26, 2021 (155)
117	14KJPN	NC_000002.12 - 21042269	Oct 12, 2022 (156)
118	TopMed	NC_000002.12 - 21042269	Apr 26, 2021 (155)
119	UK 10K study - Twins	NC_000002.11 - 21265141	Oct 11, 2018 (152)
120	A Vietnamese Genetic Variation Database	NC_000002.11 - 21265141	Jul 12, 2019 (153)
121	ALFA	NC_000002.12 - 21042269	Apr 26, 2021 (155)
122	ClinVar	RCV001553837.2	Oct 12, 2022 (156)
123	ClinVar	RCV001553838.2	Oct 12, 2022 (156)

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)
rs17240476	Mar 11, 2006 (126)
rs57596007	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss91083058, ss109290561, ss109938336, ss163180392, ss200138536, ss252965395, ss276380995, ss292525086, ss484003850, ss1585973035	NC_000002.10:21118645:C:A	NC_000002.12:21042268:C:A	(self)
7131126, 3958734, 2793154, 4950778, 1741618, 4330540, 72496, 1506170, 1846682, 3773309, 990474, 8183358, 3958734, 864882, ss219112811, ss231070873, ss238648611, ss484332152, ss536515345, ss555407878, ss648986525, ss780613886, ss782612303, ss836107323, ss976571014, ss1068922844, ss1296219074, ss1428503024, ss1578774065, ss1602976122, ss1645970155, ss1710955744, ss1796398899, ss1919804752, ss1968713783, ss2020429562, ss2094805669, ss2095088397, ss2148474120, ss2624731663, ss2633582651, ss2703034121, ss2770590086, ss2989102328, ss3344112486, ss3628009368, ss3631551433, ss3642081321, ss3646258669, ss3652376896, ss3657054906, ss3728221305, ss3756451880, ss3783799995, ss3789398118, ss3794270866, ss3826860052, ss3836836543, ss3851756329, ss3897153146, ss3984169922, ss5150214051, ss5314716540, ss5327303533, ss5506320633, ss5623919827, ss5628249052, ss5800048223, ss5800092964, ss5819763751, ss5954446895, ss5980041736, ss5981203323	NC_000002.11:21265140:C:A	NC_000002.12:21042268:C:A	(self)
RCV001553837.2, RCV001553838.2, 9470109, 3640001, 6140, 12339368, 300627617, 10970603245, ss2228150532, ss3023982342, ss3646982749, ss3703404063, ss3800835695, ss3842250884, ss3947262000, ss4496804738, ss5247184171, ss5447469719, ss5521944174, ss5678502264, ss5801993926, ss5852422432, ss5929340482	NC_000002.12:21042268:C:A	NC_000002.12:21042268:C:A	(self)
ss21641784	NT_022184.13:81074:C:A	NC_000002.12:21042268:C:A	(self)
ss834852, ss6424608, ss22886737, ss23143745, ss44351757, ss69365767, ss69369339, ss84143811, ss106074460, ss135984509, ss138402922, ss156788156, ss244305693, ss410831627	NT_022184.15:87027:C:A	NC_000002.12:21042268:C:A	(self)
4330540, ss3897153146	NC_000002.11:21265140:C:G	NC_000002.12:21042268:C:G	(self)
4330540, ss3897153146	NC_000002.11:21265140:C:T	NC_000002.12:21042268:C:T	(self)
10970603245, ss2228150532	NC_000002.12:21042268:C:T	NC_000002.12:21042268:C:T	(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 rs661665

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

rs661665