Name: rs1008375
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.

rs1008375

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:17681211 (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>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.450161 (119153/264690, TOPMED)
T=0.397704 (58484/147054, ALFA)
T=0.449088 (62902/140066, GnomAD) (+ 19 more)
T=0.15355 (4339/28258, 14KJPN)
T=0.15054 (2523/16760, 8.3KJPN)
T=0.4316 (2764/6404, 1000G_30x)
T=0.4235 (2121/5008, 1000G)
T=0.3375 (1512/4480, Estonian)
T=0.4235 (1632/3854, ALSPAC)
T=0.4080 (1513/3708, TWINSUK)
T=0.1577 (462/2930, KOREAN)
T=0.4619 (874/1892, HapMap)
T=0.1621 (297/1832, Korea1K)
T=0.403 (402/998, GoNL)
T=0.201 (158/788, PRJEB37584)
T=0.367 (220/600, NorthernSweden)
T=0.218 (107/490, SGDP_PRJ)
T=0.421 (91/216, Qatari)
T=0.208 (45/216, Vietnamese)
T=0.20 (11/54, Siberian)
T=0.33 (13/40, GENOME_DK)
T=0.33 (12/36, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM184B : 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	147054	T=0.397704	C=0.602296
European	Sub	126386	T=0.392472	C=0.607528
African	Sub	6674	T=0.6340	C=0.3660
African Others	Sub	242	T=0.723	C=0.277
African American	Sub	6432	T=0.6306	C=0.3694
Asian	Sub	630	T=0.165	C=0.835
East Asian	Sub	498	T=0.155	C=0.845
Other Asian	Sub	132	T=0.205	C=0.795
Latin American 1	Sub	750	T=0.393	C=0.607
Latin American 2	Sub	6236	T=0.2708	C=0.7292
South Asian	Sub	184	T=0.418	C=0.582
Other	Sub	6194	T=0.4012	C=0.5988

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=0.450161	C=0.549839
Allele Frequency Aggregator	Total	Global	147054	T=0.397704	C=0.602296
Allele Frequency Aggregator	European	Sub	126386	T=0.392472	C=0.607528
Allele Frequency Aggregator	African	Sub	6674	T=0.6340	C=0.3660
Allele Frequency Aggregator	Latin American 2	Sub	6236	T=0.2708	C=0.7292
Allele Frequency Aggregator	Other	Sub	6194	T=0.4012	C=0.5988
Allele Frequency Aggregator	Latin American 1	Sub	750	T=0.393	C=0.607
Allele Frequency Aggregator	Asian	Sub	630	T=0.165	C=0.835
Allele Frequency Aggregator	South Asian	Sub	184	T=0.418	C=0.582
gnomAD - Genomes	Global	Study-wide	140066	T=0.449088	C=0.550912
gnomAD - Genomes	European	Sub	75856	T=0.38302	C=0.61698
gnomAD - Genomes	African	Sub	41982	T=0.62775	C=0.37225
gnomAD - Genomes	American	Sub	13626	T=0.32754	C=0.67246
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.4961	C=0.5039
gnomAD - Genomes	East Asian	Sub	3130	T=0.1607	C=0.8393
gnomAD - Genomes	Other	Sub	2150	T=0.4093	C=0.5907
14KJPN	JAPANESE	Study-wide	28258	T=0.15355	C=0.84645
8.3KJPN	JAPANESE	Study-wide	16760	T=0.15054	C=0.84946
1000Genomes_30x	Global	Study-wide	6404	T=0.4316	C=0.5684
1000Genomes_30x	African	Sub	1786	T=0.7060	C=0.2940
1000Genomes_30x	Europe	Sub	1266	T=0.3744	C=0.6256
1000Genomes_30x	South Asian	Sub	1202	T=0.4185	C=0.5815
1000Genomes_30x	East Asian	Sub	1170	T=0.1880	C=0.8120
1000Genomes_30x	American	Sub	980	T=0.312	C=0.688
1000Genomes	Global	Study-wide	5008	T=0.4235	C=0.5765
1000Genomes	African	Sub	1322	T=0.6989	C=0.3011
1000Genomes	East Asian	Sub	1008	T=0.1875	C=0.8125
1000Genomes	Europe	Sub	1006	T=0.3698	C=0.6302
1000Genomes	South Asian	Sub	978	T=0.428	C=0.572
1000Genomes	American	Sub	694	T=0.313	C=0.687
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.3375	C=0.6625
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4235	C=0.5765
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4080	C=0.5920
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1577	A=0.0000, C=0.8423, G=0.0000
HapMap	Global	Study-wide	1892	T=0.4619	C=0.5381
HapMap	American	Sub	770	T=0.386	C=0.614
HapMap	African	Sub	692	T=0.672	C=0.328
HapMap	Asian	Sub	254	T=0.197	C=0.803
HapMap	Europe	Sub	176	T=0.352	C=0.648
Korean Genome Project	KOREAN	Study-wide	1832	T=0.1621	C=0.8379
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.403	C=0.597
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.201	C=0.799
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.201	C=0.799
Northern Sweden	ACPOP	Study-wide	600	T=0.367	C=0.633
SGDP_PRJ	Global	Study-wide	490	T=0.218	C=0.782
Qatari	Global	Study-wide	216	T=0.421	C=0.579
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.208	C=0.792
Siberian	Global	Study-wide	54	T=0.20	C=0.80
The Danish reference pan genome	Danish	Study-wide	40	T=0.33	C=0.68
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	36	T=0.33	C=0.67

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 4	NC_000004.12:g.17681211T>A
GRCh38.p14 chr 4	NC_000004.12:g.17681211T>C
GRCh38.p14 chr 4	NC_000004.12:g.17681211T>G
GRCh37.p13 chr 4	NC_000004.11:g.17682834T>A
GRCh37.p13 chr 4	NC_000004.11:g.17682834T>C
GRCh37.p13 chr 4	NC_000004.11:g.17682834T>G

Gene: FAM184B, family with sequence similarity 184 member B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM184B transcript	NM_015688.2:c.1596+7213A>T	N/A	Intron Variant
FAM184B transcript variant X1	XM_047450066.1:c.1596+721… XM_047450066.1:c.1596+7213A>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.

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=	A	C	G
GRCh38.p14 chr 4	NC_000004.12:g.17681211=	NC_000004.12:g.17681211T>A	NC_000004.12:g.17681211T>C	NC_000004.12:g.17681211T>G
GRCh37.p13 chr 4	NC_000004.11:g.17682834=	NC_000004.11:g.17682834T>A	NC_000004.11:g.17682834T>C	NC_000004.11:g.17682834T>G
FAM184B transcript	NM_015688.1:c.1596+7213=	NM_015688.1:c.1596+7213A>T	NM_015688.1:c.1596+7213A>G	NM_015688.1:c.1596+7213A>C
FAM184B transcript	NM_015688.2:c.1596+7213=	NM_015688.2:c.1596+7213A>T	NM_015688.2:c.1596+7213A>G	NM_015688.2:c.1596+7213A>C
FAM184B transcript variant X1	XM_047450066.1:c.1596+7213=	XM_047450066.1:c.1596+7213A>T	XM_047450066.1:c.1596+7213A>G	XM_047450066.1:c.1596+7213A>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#.

112 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1470665	Oct 05, 2000 (86)
2	WI_SSAHASNP	ss6471709	Feb 20, 2003 (111)
3	WI_SSAHASNP	ss11661521	Jul 11, 2003 (116)
4	ILLUMINA	ss65714082	Oct 15, 2006 (127)
5	ILLUMINA	ss75013428	Dec 06, 2007 (129)
6	HGSV	ss84232635	Dec 14, 2007 (130)
7	BCMHGSC_JDW	ss92489516	Mar 24, 2008 (129)
8	BGI	ss105809649	Feb 04, 2009 (130)
9	1000GENOMES	ss112962030	Jan 25, 2009 (130)
10	ILLUMINA-UK	ss116893904	Feb 14, 2009 (130)
11	KRIBB_YJKIM	ss119377901	Dec 01, 2009 (131)
12	ENSEMBL	ss139472066	Dec 01, 2009 (131)
13	GMI	ss156928300	Dec 01, 2009 (131)
14	ILLUMINA	ss159860839	Dec 01, 2009 (131)
15	COMPLETE_GENOMICS	ss161934158	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss163159239	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss166238821	Jul 04, 2010 (132)
18	ILLUMINA	ss169636042	Jul 04, 2010 (132)
19	BUSHMAN	ss198128678	Jul 04, 2010 (132)
20	BCM-HGSC-SUB	ss206503520	Jul 04, 2010 (132)
21	1000GENOMES	ss211366987	Jul 14, 2010 (132)
22	1000GENOMES	ss220772706	Jul 14, 2010 (132)
23	1000GENOMES	ss232282138	Jul 14, 2010 (132)
24	1000GENOMES	ss239598142	Jul 15, 2010 (132)
25	BL	ss252967278	May 09, 2011 (134)
26	GMI	ss277596574	May 04, 2012 (137)
27	GMI	ss284856536	Apr 25, 2013 (138)
28	PJP	ss293297128	May 09, 2011 (134)
29	ILLUMINA	ss479180652	May 04, 2012 (137)
30	ILLUMINA	ss479182775	May 04, 2012 (137)
31	ILLUMINA	ss479509793	Sep 08, 2015 (146)
32	ILLUMINA	ss484391363	May 04, 2012 (137)
33	ILLUMINA	ss536573918	Sep 08, 2015 (146)
34	TISHKOFF	ss557347078	Apr 25, 2013 (138)
35	SSMP	ss651111871	Apr 25, 2013 (138)
36	ILLUMINA	ss780667510	Sep 08, 2015 (146)
37	ILLUMINA	ss782642034	Sep 08, 2015 (146)
38	ILLUMINA	ss783611443	Sep 08, 2015 (146)
39	ILLUMINA	ss831892244	Sep 08, 2015 (146)
40	ILLUMINA	ss836163341	Sep 08, 2015 (146)
41	EVA-GONL	ss979824319	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1071317964	Aug 21, 2014 (142)
43	1000GENOMES	ss1308651160	Aug 21, 2014 (142)
44	DDI	ss1429791980	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1580438635	Apr 01, 2015 (144)
46	EVA_DECODE	ss1589313255	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1609525427	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1652519460	Apr 01, 2015 (144)
49	EVA_SVP	ss1712655515	Apr 01, 2015 (144)
50	ILLUMINA	ss1752510136	Sep 08, 2015 (146)
51	HAMMER_LAB	ss1801080353	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1923061940	Feb 12, 2016 (147)
53	GENOMED	ss1969672518	Jul 19, 2016 (147)
54	JJLAB	ss2022105261	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2150215653	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2260847944	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2625553895	Nov 08, 2017 (151)
58	ILLUMINA	ss2634088899	Nov 08, 2017 (151)
59	GRF	ss2705660941	Nov 08, 2017 (151)
60	GNOMAD	ss2806246176	Nov 08, 2017 (151)
61	SWEGEN	ss2994230084	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3024821999	Nov 08, 2017 (151)
63	CSHL	ss3345571880	Nov 08, 2017 (151)
64	ILLUMINA	ss3628913584	Oct 12, 2018 (152)
65	ILLUMINA	ss3632027228	Oct 12, 2018 (152)
66	ILLUMINA	ss3633327519	Oct 12, 2018 (152)
67	ILLUMINA	ss3634046259	Oct 12, 2018 (152)
68	ILLUMINA	ss3634943278	Oct 12, 2018 (152)
69	ILLUMINA	ss3635729353	Oct 12, 2018 (152)
70	ILLUMINA	ss3636644794	Oct 12, 2018 (152)
71	ILLUMINA	ss3637481851	Oct 12, 2018 (152)
72	ILLUMINA	ss3638474514	Oct 12, 2018 (152)
73	ILLUMINA	ss3640650574	Oct 12, 2018 (152)
74	ILLUMINA	ss3641160139	Oct 12, 2018 (152)
75	ILLUMINA	ss3641456940	Oct 12, 2018 (152)
76	ILLUMINA	ss3643426771	Oct 12, 2018 (152)
77	EGCUT_WGS	ss3662138790	Jul 13, 2019 (153)
78	EVA_DECODE	ss3711515451	Jul 13, 2019 (153)
79	ACPOP	ss3730905218	Jul 13, 2019 (153)
80	ILLUMINA	ss3745243570	Jul 13, 2019 (153)
81	EVA	ss3761467176	Jul 13, 2019 (153)
82	ILLUMINA	ss3772738253	Jul 13, 2019 (153)
83	PACBIO	ss3784635181	Jul 13, 2019 (153)
84	PACBIO	ss3790103854	Jul 13, 2019 (153)
85	PACBIO	ss3794978927	Jul 13, 2019 (153)
86	KHV_HUMAN_GENOMES	ss3804600000	Jul 13, 2019 (153)
87	EVA	ss3828398761	Apr 26, 2020 (154)
88	EVA	ss3837633122	Apr 26, 2020 (154)
89	EVA	ss3843067392	Apr 26, 2020 (154)
90	SGDP_PRJ	ss3858339077	Apr 26, 2020 (154)
91	KRGDB	ss3904491050	Apr 26, 2020 (154)
92	KOGIC	ss3953634320	Apr 26, 2020 (154)
93	EVA	ss3984524457	Apr 26, 2021 (155)
94	EVA	ss3985055874	Apr 26, 2021 (155)
95	EVA	ss4017134950	Apr 26, 2021 (155)
96	TOPMED	ss4604688749	Apr 26, 2021 (155)
97	TOMMO_GENOMICS	ss5164447122	Apr 26, 2021 (155)
98	1000G_HIGH_COVERAGE	ss5258237674	Oct 13, 2022 (156)
99	EVA	ss5314939832	Oct 13, 2022 (156)
100	EVA	ss5347255945	Oct 13, 2022 (156)
101	HUGCELL_USP	ss5457116493	Oct 13, 2022 (156)
102	EVA	ss5507406913	Oct 13, 2022 (156)
103	1000G_HIGH_COVERAGE	ss5538771117	Oct 13, 2022 (156)
104	SANFORD_IMAGENETICS	ss5624549038	Oct 13, 2022 (156)
105	SANFORD_IMAGENETICS	ss5634461194	Oct 13, 2022 (156)
106	TOMMO_GENOMICS	ss5698164671	Oct 13, 2022 (156)
107	EVA	ss5799608865	Oct 13, 2022 (156)
108	YY_MCH	ss5804807188	Oct 13, 2022 (156)
109	EVA	ss5843627593	Oct 13, 2022 (156)
110	EVA	ss5854103066	Oct 13, 2022 (156)
111	EVA	ss5862365431	Oct 13, 2022 (156)
112	EVA	ss5962840705	Oct 13, 2022 (156)
113	1000Genomes	NC_000004.11 - 17682834	Oct 12, 2018 (152)
114	1000Genomes_30x	NC_000004.12 - 17681211	Oct 13, 2022 (156)
115	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 17682834	Oct 12, 2018 (152)
116	Genetic variation in the Estonian population	NC_000004.11 - 17682834	Oct 12, 2018 (152)
117	The Danish reference pan genome	NC_000004.11 - 17682834	Apr 26, 2020 (154)
118	gnomAD - Genomes	NC_000004.12 - 17681211	Apr 26, 2021 (155)
119	Genome of the Netherlands Release 5	NC_000004.11 - 17682834	Apr 26, 2020 (154)
120	HapMap	NC_000004.12 - 17681211	Apr 26, 2020 (154)
121	KOREAN population from KRGDB	NC_000004.11 - 17682834	Apr 26, 2020 (154)
122	Korean Genome Project	NC_000004.12 - 17681211	Apr 26, 2020 (154)
123	Northern Sweden	NC_000004.11 - 17682834	Jul 13, 2019 (153)
124	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 17682834	Apr 26, 2021 (155)
125	CNV burdens in cranial meningiomas	NC_000004.11 - 17682834	Apr 26, 2021 (155)
126	Qatari	NC_000004.11 - 17682834	Apr 26, 2020 (154)
127	SGDP_PRJ	NC_000004.11 - 17682834	Apr 26, 2020 (154)
128	Siberian	NC_000004.11 - 17682834	Apr 26, 2020 (154)
129	8.3KJPN	NC_000004.11 - 17682834	Apr 26, 2021 (155)
130	14KJPN	NC_000004.12 - 17681211	Oct 13, 2022 (156)
131	TopMed	NC_000004.12 - 17681211	Apr 26, 2021 (155)
132	UK 10K study - Twins	NC_000004.11 - 17682834	Oct 12, 2018 (152)
133	A Vietnamese Genetic Variation Database	NC_000004.11 - 17682834	Jul 13, 2019 (153)
134	ALFA	NC_000004.12 - 17681211	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)
rs57657620	May 24, 2008 (130)
rs386509602	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11668444, ss3904491050	NC_000004.11:17682833:T:A	NC_000004.12:17681210:T:A	(self)
ss84232635	NC_000004.9:17359102:T:C	NC_000004.12:17681210:T:C	(self)
ss92489516, ss112962030, ss116893904, ss161934158, ss163159239, ss166238821, ss198128678, ss206503520, ss211366987, ss252967278, ss277596574, ss284856536, ss293297128, ss479180652, ss1589313255, ss1712655515, ss3643426771	NC_000004.10:17291931:T:C	NC_000004.12:17681210:T:C	(self)
20006315, 11143333, 7877038, 6603574, 4903772, 11668444, 4190083, 281801, 73816, 5103870, 10356057, 2732007, 22416429, 11143333, 2435598, ss220772706, ss232282138, ss239598142, ss479182775, ss479509793, ss484391363, ss536573918, ss557347078, ss651111871, ss780667510, ss782642034, ss783611443, ss831892244, ss836163341, ss979824319, ss1071317964, ss1308651160, ss1429791980, ss1580438635, ss1609525427, ss1652519460, ss1752510136, ss1801080353, ss1923061940, ss1969672518, ss2022105261, ss2150215653, ss2625553895, ss2634088899, ss2705660941, ss2806246176, ss2994230084, ss3345571880, ss3628913584, ss3632027228, ss3633327519, ss3634046259, ss3634943278, ss3635729353, ss3636644794, ss3637481851, ss3638474514, ss3640650574, ss3641160139, ss3641456940, ss3662138790, ss3730905218, ss3745243570, ss3761467176, ss3772738253, ss3784635181, ss3790103854, ss3794978927, ss3828398761, ss3837633122, ss3858339077, ss3904491050, ss3984524457, ss3985055874, ss4017134950, ss5164447122, ss5314939832, ss5347255945, ss5507406913, ss5624549038, ss5634461194, ss5799608865, ss5843627593, ss5962840705	NC_000004.11:17682833:T:C	NC_000004.12:17681210:T:C	(self)
26297052, 141795276, 2567018, 10012321, 32001775, 442066305, 3445486484, ss2260847944, ss3024821999, ss3711515451, ss3804600000, ss3843067392, ss3953634320, ss4604688749, ss5258237674, ss5457116493, ss5538771117, ss5698164671, ss5804807188, ss5854103066, ss5862365431	NC_000004.12:17681210:T:C	NC_000004.12:17681210:T:C	(self)
ss11661521	NT_006316.15:8358191:T:C	NC_000004.12:17681210:T:C	(self)
ss1470665, ss6471709, ss65714082, ss75013428, ss105809649, ss119377901, ss139472066, ss156928300, ss159860839, ss169636042	NT_006316.16:8864630:T:C	NC_000004.12:17681210:T:C	(self)
11668444, ss3904491050	NC_000004.11:17682833:T:G	NC_000004.12:17681210:T:G	(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 rs1008375

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

rs1008375