Name: rs17495612
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.

rs17495612

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:32391654 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.143439 (37967/264690, TOPMED)
C=0.155531 (21780/140036, GnomAD)
C=0.13870 (6190/44628, ALFA) (+ 18 more)
C=0.28495 (8052/28258, 14KJPN)
C=0.28496 (4776/16760, 8.3KJPN)
C=0.1658 (1062/6404, 1000G_30x)
C=0.1681 (842/5008, 1000G)
C=0.1688 (756/4480, Estonian)
C=0.1334 (514/3854, ALSPAC)
C=0.1206 (447/3708, TWINSUK)
C=0.2298 (671/2920, KOREAN)
C=0.1494 (282/1888, HapMap)
C=0.1276 (145/1136, Daghestan)
C=0.130 (130/998, GoNL)
C=0.145 (87/600, NorthernSweden)
C=0.106 (23/216, Qatari)
C=0.066 (14/212, Vietnamese)
T=0.469 (76/162, SGDP_PRJ)
C=0.10 (4/40, GENOME_DK)
T=0.50 (9/18, Siberian)
C=0.50 (9/18, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HCG23 : Non Coding Transcript Variant
TSBP1-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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	44628	T=0.86130	C=0.13870
European	Sub	28114	T=0.86224	C=0.13776
African	Sub	4114	T=0.8551	C=0.1449
African Others	Sub	136	T=0.816	C=0.184
African American	Sub	3978	T=0.8565	C=0.1435
Asian	Sub	196	T=0.913	C=0.087
East Asian	Sub	132	T=0.886	C=0.114
Other Asian	Sub	64	T=0.97	C=0.03
Latin American 1	Sub	380	T=0.868	C=0.132
Latin American 2	Sub	6872	T=0.8612	C=0.1388
South Asian	Sub	142	T=0.866	C=0.134
Other	Sub	4810	T=0.8584	C=0.1416

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	T=0.856561	C=0.143439
gnomAD - Genomes	Global	Study-wide	140036	T=0.844469	C=0.155531
gnomAD - Genomes	European	Sub	75806	T=0.83451	C=0.16549
gnomAD - Genomes	African	Sub	41976	T=0.84910	C=0.15090
gnomAD - Genomes	American	Sub	13660	T=0.85915	C=0.14085
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.9205	C=0.0795
gnomAD - Genomes	East Asian	Sub	3128	T=0.8798	C=0.1202
gnomAD - Genomes	Other	Sub	2144	T=0.8428	C=0.1572
Allele Frequency Aggregator	Total	Global	44628	T=0.86130	C=0.13870
Allele Frequency Aggregator	European	Sub	28114	T=0.86224	C=0.13776
Allele Frequency Aggregator	Latin American 2	Sub	6872	T=0.8612	C=0.1388
Allele Frequency Aggregator	Other	Sub	4810	T=0.8584	C=0.1416
Allele Frequency Aggregator	African	Sub	4114	T=0.8551	C=0.1449
Allele Frequency Aggregator	Latin American 1	Sub	380	T=0.868	C=0.132
Allele Frequency Aggregator	Asian	Sub	196	T=0.913	C=0.087
Allele Frequency Aggregator	South Asian	Sub	142	T=0.866	C=0.134
14KJPN	JAPANESE	Study-wide	28258	T=0.71505	C=0.28495
8.3KJPN	JAPANESE	Study-wide	16760	T=0.71504	C=0.28496
1000Genomes_30x	Global	Study-wide	6404	T=0.8342	C=0.1658
1000Genomes_30x	African	Sub	1786	T=0.8432	C=0.1568
1000Genomes_30x	Europe	Sub	1266	T=0.8365	C=0.1635
1000Genomes_30x	South Asian	Sub	1202	T=0.7987	C=0.2013
1000Genomes_30x	East Asian	Sub	1170	T=0.8547	C=0.1453
1000Genomes_30x	American	Sub	980	T=0.834	C=0.166
1000Genomes	Global	Study-wide	5008	T=0.8319	C=0.1681
1000Genomes	African	Sub	1322	T=0.8419	C=0.1581
1000Genomes	East Asian	Sub	1008	T=0.8442	C=0.1558
1000Genomes	Europe	Sub	1006	T=0.8370	C=0.1630
1000Genomes	South Asian	Sub	978	T=0.798	C=0.202
1000Genomes	American	Sub	694	T=0.836	C=0.164
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8313	C=0.1688
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8666	C=0.1334
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8794	C=0.1206
KOREAN population from KRGDB	KOREAN	Study-wide	2920	T=0.7702	C=0.2298
HapMap	Global	Study-wide	1888	T=0.8506	C=0.1494
HapMap	American	Sub	768	T=0.858	C=0.142
HapMap	African	Sub	692	T=0.882	C=0.118
HapMap	Asian	Sub	252	T=0.722	C=0.278
HapMap	Europe	Sub	176	T=0.881	C=0.119
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	T=0.8724	C=0.1276
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.895	C=0.105
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.854	C=0.146
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.828	C=0.172
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.843	C=0.157
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.83	C=0.17
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.92	C=0.08
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.870	C=0.130
Northern Sweden	ACPOP	Study-wide	600	T=0.855	C=0.145
Qatari	Global	Study-wide	216	T=0.894	C=0.106
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.934	C=0.066
SGDP_PRJ	Global	Study-wide	162	T=0.469	C=0.531
The Danish reference pan genome	Danish	Study-wide	40	T=0.90	C=0.10
Siberian	Global	Study-wide	18	T=0.50	C=0.50

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 6	NC_000006.12:g.32391654T>C
GRCh37.p13 chr 6	NC_000006.11:g.32359431T>C
BTNL2 RefSeqGene	NG_054759.1:g.22226A>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3829754T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3829860T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.2:g.3723885T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.1:g.3673801T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.3614694T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.3620290T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.3696647T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.3702267T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.3707576T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.3706874T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.3733404T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.3738989T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.3632745T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.3638330T>C
GRCh38.p14 chr 6 alt locus HSCHR6_8_CTG1	NT_187692.1:g.62306G>A

Gene: HCG23, HLA complex group 23 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HCG23 transcript	NR_044996.1:n.286T>C	N/A	Non Coding Transcript Variant

Gene: TSBP1-AS1, TSBP1 and BTNL2 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TSBP1-AS1 transcript variant 2	NR_136245.1:n.	N/A	Intron Variant
TSBP1-AS1 transcript variant 1	NR_136244.1:n.	N/A	Genic Downstream Transcript Variant
TSBP1-AS1 transcript variant 3	NR_136246.1: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	T=	C
GRCh38.p14 chr 6	NC_000006.12:g.32391654=	NC_000006.12:g.32391654T>C
GRCh37.p13 chr 6	NC_000006.11:g.32359431=	NC_000006.11:g.32359431T>C
BTNL2 RefSeqGene	NG_054759.1:g.22226=	NG_054759.1:g.22226A>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.3829754=	NT_113891.3:g.3829754T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.3829860=	NT_113891.2:g.3829860T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.2:g.3723885=	NT_167244.2:g.3723885T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1	NT_167244.1:g.3673801=	NT_167244.1:g.3673801T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.3614694=	NT_167248.2:g.3614694T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.3620290=	NT_167248.1:g.3620290T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.3696647=	NT_167246.2:g.3696647T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.3702267=	NT_167246.1:g.3702267T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.3707576=	NT_167249.2:g.3707576T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.3706874=	NT_167249.1:g.3706874T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.3733404=	NT_167247.2:g.3733404T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.3738989=	NT_167247.1:g.3738989T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.2:g.3632745=	NT_167245.2:g.3632745T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1	NT_167245.1:g.3638330=	NT_167245.1:g.3638330T>C
GRCh38.p14 chr 6 alt locus HSCHR6_8_CTG1	NT_187692.1:g.62306G>A	NT_187692.1:g.62306=
HCG23 transcript	NR_044996.1:n.286=	NR_044996.1:n.286T>C

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#.

71 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24650829	Sep 20, 2004 (123)
2	AFFY	ss66442026	Nov 29, 2006 (127)
3	AFFY	ss76224137	Dec 06, 2007 (129)
4	KRIBB_YJKIM	ss83250621	Dec 16, 2007 (130)
5	BCMHGSC_JDW	ss93437712	Mar 24, 2008 (129)
6	1000GENOMES	ss109906020	Feb 13, 2009 (137)
7	1000GENOMES	ss114151530	Jan 25, 2009 (137)
8	ILLUMINA	ss160445595	Dec 01, 2009 (131)
9	COMPLETE_GENOMICS	ss163354245	Jul 04, 2010 (132)
10	AFFY	ss172875504	Jul 04, 2010 (132)
11	BCM-HGSC-SUB	ss207731855	Jul 04, 2010 (132)
12	1000GENOMES	ss222306801	Jul 14, 2010 (137)
13	1000GENOMES	ss233401664	Jul 14, 2010 (137)
14	1000GENOMES	ss240472228	Jul 15, 2010 (137)
15	GMI	ss278730116	May 04, 2012 (137)
16	ILLUMINA	ss480998434	Sep 08, 2015 (146)
17	ILLUMINA	ss536321075	Sep 08, 2015 (146)
18	SSMP	ss653040179	Apr 25, 2013 (138)
19	ILLUMINA	ss778697005	Sep 08, 2015 (146)
20	ILLUMINA	ss834155850	Sep 08, 2015 (146)
21	EVA-GONL	ss982773096	Aug 21, 2014 (142)
22	JMKIDD_LAB	ss1073510015	Aug 21, 2014 (142)
23	1000GENOMES	ss1319578098	Aug 21, 2014 (142)
24	HAMMER_LAB	ss1397450591	Sep 08, 2015 (146)
25	EVA_GENOME_DK	ss1581609748	Apr 01, 2015 (144)
26	EVA_UK10K_ALSPAC	ss1615288478	Apr 01, 2015 (144)
27	EVA_UK10K_TWINSUK	ss1658282511	Apr 01, 2015 (144)
28	EVA_SVP	ss1712852050	Apr 01, 2015 (144)
29	HAMMER_LAB	ss1804360767	Sep 08, 2015 (146)
30	WEILL_CORNELL_DGM	ss1926025096	Feb 12, 2016 (147)
31	JJLAB	ss2023646405	Sep 14, 2016 (149)
32	USC_VALOUEV	ss2151813617	Dec 20, 2016 (150)
33	HUMAN_LONGEVITY	ss2282982119	Dec 20, 2016 (150)
34	ILLUMINA	ss2634432263	Nov 08, 2017 (151)
35	GRF	ss2707407570	Nov 08, 2017 (151)
36	AFFY	ss2985995596	Nov 08, 2017 (151)
37	SWEGEN	ss2998807182	Nov 08, 2017 (151)
38	BIOINF_KMB_FNS_UNIBA	ss3025610326	Nov 08, 2017 (151)
39	ILLUMINA	ss3629508366	Oct 12, 2018 (152)
40	ILLUMINA	ss3632350488	Oct 12, 2018 (152)
41	ILLUMINA	ss3636780168	Oct 12, 2018 (152)
42	EGCUT_WGS	ss3666720561	Jul 13, 2019 (153)
43	EVA_DECODE	ss3716920961	Jul 13, 2019 (153)
44	ACPOP	ss3733368069	Jul 13, 2019 (153)
45	EVA	ss3764830499	Jul 13, 2019 (153)
46	KHV_HUMAN_GENOMES	ss3807985175	Jul 13, 2019 (153)
47	EVA	ss3829836522	Apr 26, 2020 (154)
48	EVA	ss3838396800	Apr 26, 2020 (154)
49	EVA	ss3843839000	Apr 26, 2020 (154)
50	SGDP_PRJ	ss3864267150	Apr 26, 2020 (154)
51	KRGDB	ss3911044530	Apr 26, 2020 (154)
52	VINODS	ss4025172227	Apr 26, 2021 (155)
53	VINODS	ss4025190241	Apr 26, 2021 (155)
54	VINODS	ss4025210693	Apr 26, 2021 (155)
55	VINODS	ss4025230576	Apr 26, 2021 (155)
56	VINODS	ss4025249403	Apr 26, 2021 (155)
57	VINODS	ss4025268210	Apr 26, 2021 (155)
58	VINODS	ss4025289037	Apr 26, 2021 (155)
59	TOPMED	ss4698551433	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5176862800	Apr 26, 2021 (155)
61	1000G_HIGH_COVERAGE	ss5267955342	Oct 13, 2022 (156)
62	EVA	ss5364754631	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5465686801	Oct 13, 2022 (156)
64	EVA	ss5508432504	Oct 13, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5553618777	Oct 13, 2022 (156)
66	SANFORD_IMAGENETICS	ss5640100751	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5714726390	Oct 13, 2022 (156)
68	YY_MCH	ss5807314442	Oct 13, 2022 (156)
69	EVA	ss5842036385	Oct 13, 2022 (156)
70	EVA	ss5883263140	Oct 13, 2022 (156)
71	EVA	ss5968602574	Oct 13, 2022 (156)
72	1000Genomes	NC_000006.11 - 32359431	Oct 12, 2018 (152)
73	1000Genomes_30x	NC_000006.12 - 32391654	Oct 13, 2022 (156)
74	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 32359431	Oct 12, 2018 (152)
75	Genome-wide autozygosity in Daghestan	NC_000006.10 - 32467409	Apr 26, 2020 (154)
76	Genetic variation in the Estonian population	NC_000006.11 - 32359431	Oct 12, 2018 (152)
77	The Danish reference pan genome	NC_000006.11 - 32359431	Apr 26, 2020 (154)
78	gnomAD - Genomes	NC_000006.12 - 32391654	Apr 26, 2021 (155)
79	Genome of the Netherlands Release 5	NC_000006.11 - 32359431	Apr 26, 2020 (154)
80	HapMap	NC_000006.12 - 32391654	Apr 26, 2020 (154)
81	KOREAN population from KRGDB	NC_000006.11 - 32359431	Apr 26, 2020 (154)
82	Northern Sweden	NC_000006.11 - 32359431	Jul 13, 2019 (153)
83	Qatari	NC_000006.11 - 32359431	Apr 26, 2020 (154)
84	SGDP_PRJ	NC_000006.11 - 32359431	Apr 26, 2020 (154)
85	Siberian	NC_000006.11 - 32359431	Apr 26, 2020 (154)
86	8.3KJPN	NC_000006.11 - 32359431	Apr 26, 2021 (155)
87	14KJPN	NC_000006.12 - 32391654	Oct 13, 2022 (156)
88	TopMed	NC_000006.12 - 32391654	Apr 26, 2021 (155)
89	UK 10K study - Twins	NC_000006.11 - 32359431	Oct 12, 2018 (152)
90	A Vietnamese Genetic Variation Database	NC_000006.11 - 32359431	Jul 13, 2019 (153)
91	ALFA	NC_000006.12 - 32391654	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)
rs61341721	Feb 27, 2009 (130)
rs114410586	May 04, 2012 (137)
rs118130747	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
425239, ss93437712, ss109906020, ss114151530, ss163354245, ss207731855, ss278730116, ss1397450591, ss1712852050	NC_000006.10:32467408:T:C	NC_000006.12:32391653:T:C	(self)
31346409, 17479360, 12458809, 7774687, 7771431, 18221924, 6652934, 8067026, 16284130, 4329971, 34832107, 17479360, 3877078, ss222306801, ss233401664, ss240472228, ss480998434, ss536321075, ss653040179, ss778697005, ss834155850, ss982773096, ss1073510015, ss1319578098, ss1581609748, ss1615288478, ss1658282511, ss1804360767, ss1926025096, ss2023646405, ss2151813617, ss2634432263, ss2707407570, ss2985995596, ss2998807182, ss3629508366, ss3632350488, ss3636780168, ss3666720561, ss3733368069, ss3764830499, ss3829836522, ss3838396800, ss3864267150, ss3911044530, ss5176862800, ss5364754631, ss5508432504, ss5640100751, ss5842036385, ss5968602574	NC_000006.11:32359430:T:C	NC_000006.12:32391653:T:C	(self)
41144712, 221362622, 3101862, 48563494, 535928991, 110132323, ss2282982119, ss3025610326, ss3716920961, ss3807985175, ss3843839000, ss4698551433, ss5267955342, ss5465686801, ss5553618777, ss5714726390, ss5807314442, ss5883263140	NC_000006.12:32391653:T:C	NC_000006.12:32391653:T:C	(self)
ss24650829, ss66442026, ss76224137, ss83250621, ss160445595, ss172875504	NT_007592.15:32299430:T:C	NC_000006.12:32391653:T:C	(self)
ss4025190241	NT_113891.3:3829753:T:C	NC_000006.12:32391653:T:C	(self)
ss4025172227	NT_167244.2:3723884:T:C	NC_000006.12:32391653:T:C	(self)
ss4025210693	NT_167245.2:3632744:T:C	NC_000006.12:32391653:T:C	(self)
ss4025230576	NT_167246.2:3696646:T:C	NC_000006.12:32391653:T:C	(self)
ss4025249403	NT_167247.2:3733403:T:C	NC_000006.12:32391653:T:C	(self)
ss4025268210	NT_167248.2:3614693:T:C	NC_000006.12:32391653:T:C	(self)
ss4025289037	NT_167249.2:3707575:T:C	NC_000006.12:32391653:T:C	(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 rs17495612

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

rs17495612