Name: rs1575667
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.

rs1575667

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:23665686 (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: A>C / A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.130961 (34664/264690, TOPMED)
A=0.136022 (19052/140066, GnomAD)
A=0.24959 (7053/28258, 14KJPN) (+ 17 more)
A=0.11992 (2278/18996, ALFA)
A=0.25101 (4207/16760, 8.3KJPN)
A=0.1651 (1057/6404, 1000G_30x)
A=0.1713 (858/5008, 1000G)
A=0.0859 (385/4480, Estonian)
A=0.1183 (456/3854, ALSPAC)
A=0.1230 (456/3708, TWINSUK)
A=0.1860 (545/2930, KOREAN)
A=0.1162 (132/1136, Daghestan)
A=0.139 (139/998, GoNL)
A=0.158 (95/600, NorthernSweden)
A=0.118 (63/536, SGDP_PRJ)
A=0.192 (58/302, HapMap)
A=0.134 (29/216, Qatari)
A=0.157 (34/216, Vietnamese)
A=0.09 (5/54, Siberian)
A=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TNFRSF19 : 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	18996	A=0.11992	C=0.88008
European	Sub	14370	A=0.11079	C=0.88921
African	Sub	2950	A=0.1644	C=0.8356
African Others	Sub	114	A=0.219	C=0.781
African American	Sub	2836	A=0.1622	C=0.8378
Asian	Sub	114	A=0.088	C=0.912
East Asian	Sub	88	A=0.08	C=0.92
Other Asian	Sub	26	A=0.12	C=0.88
Latin American 1	Sub	146	A=0.130	C=0.870
Latin American 2	Sub	610	A=0.087	C=0.913
South Asian	Sub	100	A=0.26	C=0.74
Other	Sub	706	A=0.132	C=0.868

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	A=0.130961	C=0.869039
gnomAD - Genomes	Global	Study-wide	140066	A=0.136022	C=0.863978
gnomAD - Genomes	European	Sub	75872	A=0.12335	C=0.87665
gnomAD - Genomes	African	Sub	41938	A=0.17140	C=0.82860
gnomAD - Genomes	American	Sub	13654	A=0.09426	C=0.90574
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.1183	C=0.8817
gnomAD - Genomes	East Asian	Sub	3130	A=0.1681	C=0.8319
gnomAD - Genomes	Other	Sub	2150	A=0.1391	C=0.8609
14KJPN	JAPANESE	Study-wide	28258	A=0.24959	C=0.75041
Allele Frequency Aggregator	Total	Global	18996	A=0.11992	C=0.88008
Allele Frequency Aggregator	European	Sub	14370	A=0.11079	C=0.88921
Allele Frequency Aggregator	African	Sub	2950	A=0.1644	C=0.8356
Allele Frequency Aggregator	Other	Sub	706	A=0.132	C=0.868
Allele Frequency Aggregator	Latin American 2	Sub	610	A=0.087	C=0.913
Allele Frequency Aggregator	Latin American 1	Sub	146	A=0.130	C=0.870
Allele Frequency Aggregator	Asian	Sub	114	A=0.088	C=0.912
Allele Frequency Aggregator	South Asian	Sub	100	A=0.26	C=0.74
8.3KJPN	JAPANESE	Study-wide	16760	A=0.25101	C=0.74899
1000Genomes_30x	Global	Study-wide	6404	A=0.1651	C=0.8349
1000Genomes_30x	African	Sub	1786	A=0.1741	C=0.8259
1000Genomes_30x	Europe	Sub	1266	A=0.1382	C=0.8618
1000Genomes_30x	South Asian	Sub	1202	A=0.2321	C=0.7679
1000Genomes_30x	East Asian	Sub	1170	A=0.1786	C=0.8214
1000Genomes_30x	American	Sub	980	A=0.085	C=0.915
1000Genomes	Global	Study-wide	5008	A=0.1713	C=0.8287
1000Genomes	African	Sub	1322	A=0.1785	C=0.8215
1000Genomes	East Asian	Sub	1008	A=0.1855	C=0.8145
1000Genomes	Europe	Sub	1006	A=0.1362	C=0.8638
1000Genomes	South Asian	Sub	978	A=0.240	C=0.760
1000Genomes	American	Sub	694	A=0.091	C=0.909
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.0859	C=0.9141
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.1183	C=0.8817
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.1230	C=0.8770
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.1860	C=0.8140, G=0.0000
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	A=0.1162	C=0.8838
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.083	C=0.917
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.090	C=0.910
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.205	C=0.795
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.139	C=0.861
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.19	C=0.81
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.22	C=0.78
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.139	C=0.861
Northern Sweden	ACPOP	Study-wide	600	A=0.158	C=0.842
SGDP_PRJ	Global	Study-wide	536	A=0.118	C=0.882
HapMap	Global	Study-wide	302	A=0.192	C=0.808
HapMap	African	Sub	116	A=0.147	C=0.853
HapMap	American	Sub	112	A=0.170	C=0.830
HapMap	Asian	Sub	74	A=0.30	C=0.70
Qatari	Global	Study-wide	216	A=0.134	C=0.866
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.157	C=0.843
Siberian	Global	Study-wide	54	A=0.09	C=0.91
The Danish reference pan genome	Danish	Study-wide	40	A=0.10	C=0.90

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 13	NC_000013.11:g.23665686A>C
GRCh38.p14 chr 13	NC_000013.11:g.23665686A>G
GRCh37.p13 chr 13	NC_000013.10:g.24239825A>C
GRCh37.p13 chr 13	NC_000013.10:g.24239825A>G

Gene: TNFRSF19, TNF receptor superfamily member 19 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TNFRSF19 transcript variant 3	NM_001204458.3:c.737-2294… NM_001204458.3:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant 4	NM_001204459.2:c.341-2294… NM_001204459.2:c.341-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant 5	NM_001354985.2:c.737-2294… NM_001354985.2:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant 1	NM_018647.5:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant 2	NM_148957.4:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant X3	XM_005266446.3:c.737-2294… XM_005266446.3:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant X1	XM_047430440.1:c.737-2294… XM_047430440.1:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant X2	XM_047430441.1:c.737-2294… XM_047430441.1:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant X4	XM_047430442.1:c.737-2294… XM_047430442.1:c.737-2294A>C	N/A	Intron Variant
TNFRSF19 transcript variant X5	XM_047430443.1:c.737-2294… XM_047430443.1:c.737-2294A>C	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	A=	C	G
GRCh38.p14 chr 13	NC_000013.11:g.23665686=	NC_000013.11:g.23665686A>C	NC_000013.11:g.23665686A>G
GRCh37.p13 chr 13	NC_000013.10:g.24239825=	NC_000013.10:g.24239825A>C	NC_000013.10:g.24239825A>G
TNFRSF19 transcript variant 3	NM_001204458.1:c.737-2294=	NM_001204458.1:c.737-2294A>C	NM_001204458.1:c.737-2294A>G
TNFRSF19 transcript variant 3	NM_001204458.3:c.737-2294=	NM_001204458.3:c.737-2294A>C	NM_001204458.3:c.737-2294A>G
TNFRSF19 transcript variant 4	NM_001204459.1:c.341-2294=	NM_001204459.1:c.341-2294A>C	NM_001204459.1:c.341-2294A>G
TNFRSF19 transcript variant 4	NM_001204459.2:c.341-2294=	NM_001204459.2:c.341-2294A>C	NM_001204459.2:c.341-2294A>G
TNFRSF19 transcript variant 5	NM_001354985.2:c.737-2294=	NM_001354985.2:c.737-2294A>C	NM_001354985.2:c.737-2294A>G
TNFRSF19 transcript variant 1	NM_018647.3:c.737-2294=	NM_018647.3:c.737-2294A>C	NM_018647.3:c.737-2294A>G
TNFRSF19 transcript variant 1	NM_018647.5:c.737-2294=	NM_018647.5:c.737-2294A>C	NM_018647.5:c.737-2294A>G
TNFRSF19 transcript variant 2	NM_148957.3:c.737-2294=	NM_148957.3:c.737-2294A>C	NM_148957.3:c.737-2294A>G
TNFRSF19 transcript variant 2	NM_148957.4:c.737-2294=	NM_148957.4:c.737-2294A>C	NM_148957.4:c.737-2294A>G
TNFRSF19 transcript variant X1	XM_005266445.1:c.737-2294=	XM_005266445.1:c.737-2294A>C	XM_005266445.1:c.737-2294A>G
TNFRSF19 transcript variant X4	XM_005266446.1:c.737-2294=	XM_005266446.1:c.737-2294A>C	XM_005266446.1:c.737-2294A>G
TNFRSF19 transcript variant X3	XM_005266446.3:c.737-2294=	XM_005266446.3:c.737-2294A>C	XM_005266446.3:c.737-2294A>G
TNFRSF19 transcript variant X1	XM_047430440.1:c.737-2294=	XM_047430440.1:c.737-2294A>C	XM_047430440.1:c.737-2294A>G
TNFRSF19 transcript variant X2	XM_047430441.1:c.737-2294=	XM_047430441.1:c.737-2294A>C	XM_047430441.1:c.737-2294A>G
TNFRSF19 transcript variant X4	XM_047430442.1:c.737-2294=	XM_047430442.1:c.737-2294A>C	XM_047430442.1:c.737-2294A>G
TNFRSF19 transcript variant X5	XM_047430443.1:c.737-2294=	XM_047430443.1:c.737-2294A>C	XM_047430443.1:c.737-2294A>G

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#.

81 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2094992	Oct 24, 2000 (88)
2	SC_JCM	ss6227730	Feb 20, 2003 (111)
3	BCM_SSAHASNP	ss11065147	Jul 11, 2003 (116)
4	SC_SNP	ss13167363	Dec 05, 2003 (119)
5	CSHL-HAPMAP	ss19265408	Feb 27, 2004 (120)
6	CSHL-HAPMAP	ss19961924	Feb 27, 2004 (120)
7	SSAHASNP	ss21135734	Apr 05, 2004 (121)
8	HGSV	ss77337841	Dec 07, 2007 (129)
9	HGSV	ss81352708	Dec 15, 2007 (130)
10	HGSV	ss85088701	Dec 15, 2007 (130)
11	BCMHGSC_JDW	ss89529637	Mar 24, 2008 (129)
12	BGI	ss103102079	Dec 01, 2009 (131)
13	1000GENOMES	ss112610678	Jan 25, 2009 (130)
14	1000GENOMES	ss114406131	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss118385660	Feb 14, 2009 (130)
16	ENSEMBL	ss133480589	Dec 01, 2009 (131)
17	GMI	ss154522919	Dec 01, 2009 (131)
18	ENSEMBL	ss161581355	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss167693477	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss168945832	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss170870308	Jul 04, 2010 (132)
22	BUSHMAN	ss198962387	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss208520948	Jul 04, 2010 (132)
24	1000GENOMES	ss226075931	Jul 14, 2010 (132)
25	1000GENOMES	ss236173337	Jul 15, 2010 (132)
26	1000GENOMES	ss242684503	Jul 15, 2010 (132)
27	BL	ss254846136	May 09, 2011 (134)
28	GMI	ss281635712	May 04, 2012 (137)
29	GMI	ss286666565	Apr 25, 2013 (138)
30	PJP	ss291555302	May 09, 2011 (134)
31	TISHKOFF	ss563545221	Apr 25, 2013 (138)
32	SSMP	ss659138935	Apr 25, 2013 (138)
33	EVA-GONL	ss990185463	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1078931977	Aug 21, 2014 (142)
35	1000GENOMES	ss1347469519	Aug 21, 2014 (142)
36	HAMMER_LAB	ss1397651755	Sep 08, 2015 (146)
37	DDI	ss1427125378	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1576667582	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1629876682	Apr 01, 2015 (144)
40	EVA_DECODE	ss1642291396	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1672870715	Apr 01, 2015 (144)
42	HAMMER_LAB	ss1807522170	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1933553247	Feb 12, 2016 (147)
44	GENOMED	ss1967732158	Jul 19, 2016 (147)
45	JJLAB	ss2027530740	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2155894198	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2194823427	Dec 20, 2016 (150)
48	SYSTEMSBIOZJU	ss2628252651	Nov 08, 2017 (151)
49	GRF	ss2700265348	Nov 08, 2017 (151)
50	GNOMAD	ss2917531730	Nov 08, 2017 (151)
51	SWEGEN	ss3010709898	Nov 08, 2017 (151)
52	BIOINF_KMB_FNS_UNIBA	ss3027579693	Nov 08, 2017 (151)
53	CSHL	ss3350361107	Nov 08, 2017 (151)
54	URBANLAB	ss3649985779	Oct 12, 2018 (152)
55	EGCUT_WGS	ss3677977311	Jul 13, 2019 (153)
56	EVA_DECODE	ss3694912292	Jul 13, 2019 (153)
57	ACPOP	ss3739576046	Jul 13, 2019 (153)
58	EVA	ss3751227035	Jul 13, 2019 (153)
59	PACBIO	ss3787401268	Jul 13, 2019 (153)
60	PACBIO	ss3792475422	Jul 13, 2019 (153)
61	PACBIO	ss3797359115	Jul 13, 2019 (153)
62	KHV_HUMAN_GENOMES	ss3816558085	Jul 13, 2019 (153)
63	EVA	ss3833444013	Apr 27, 2020 (154)
64	EVA	ss3840297578	Apr 27, 2020 (154)
65	EVA	ss3845781949	Apr 27, 2020 (154)
66	SGDP_PRJ	ss3879579193	Apr 27, 2020 (154)
67	KRGDB	ss3928395051	Apr 27, 2020 (154)
68	TOPMED	ss4939751045	Apr 26, 2021 (155)
69	TOMMO_GENOMICS	ss5209149843	Apr 26, 2021 (155)
70	1000G_HIGH_COVERAGE	ss5293073691	Oct 16, 2022 (156)
71	EVA	ss5409569853	Oct 16, 2022 (156)
72	HUGCELL_USP	ss5487504269	Oct 16, 2022 (156)
73	EVA	ss5510905263	Oct 16, 2022 (156)
74	1000G_HIGH_COVERAGE	ss5591699009	Oct 16, 2022 (156)
75	SANFORD_IMAGENETICS	ss5654387371	Oct 16, 2022 (156)
76	TOMMO_GENOMICS	ss5760783626	Oct 16, 2022 (156)
77	YY_MCH	ss5813942906	Oct 16, 2022 (156)
78	EVA	ss5839212006	Oct 16, 2022 (156)
79	EVA	ss5850644182	Oct 16, 2022 (156)
80	EVA	ss5924345266	Oct 16, 2022 (156)
81	EVA	ss5945792764	Oct 16, 2022 (156)
82	1000Genomes	NC_000013.10 - 24239825	Oct 12, 2018 (152)
83	1000Genomes_30x	NC_000013.11 - 23665686	Oct 16, 2022 (156)
84	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 24239825	Oct 12, 2018 (152)
85	Genome-wide autozygosity in Daghestan	NC_000013.9 - 23137825	Apr 27, 2020 (154)
86	Genetic variation in the Estonian population	NC_000013.10 - 24239825	Oct 12, 2018 (152)
87	The Danish reference pan genome	NC_000013.10 - 24239825	Apr 27, 2020 (154)
88	gnomAD - Genomes	NC_000013.11 - 23665686	Apr 26, 2021 (155)
89	Genome of the Netherlands Release 5	NC_000013.10 - 24239825	Apr 27, 2020 (154)
90	HapMap	NC_000013.11 - 23665686	Apr 27, 2020 (154)
91	KOREAN population from KRGDB	NC_000013.10 - 24239825	Apr 27, 2020 (154)
92	Northern Sweden	NC_000013.10 - 24239825	Jul 13, 2019 (153)
93	Qatari	NC_000013.10 - 24239825	Apr 27, 2020 (154)
94	SGDP_PRJ	NC_000013.10 - 24239825	Apr 27, 2020 (154)
95	Siberian	NC_000013.10 - 24239825	Apr 27, 2020 (154)
96	8.3KJPN	NC_000013.10 - 24239825	Apr 26, 2021 (155)
97	14KJPN	NC_000013.11 - 23665686	Oct 16, 2022 (156)
98	TopMed	NC_000013.11 - 23665686	Apr 26, 2021 (155)
99	UK 10K study - Twins	NC_000013.10 - 24239825	Oct 12, 2018 (152)
100	A Vietnamese Genetic Variation Database	NC_000013.10 - 24239825	Jul 13, 2019 (153)
101	ALFA	NC_000013.11 - 23665686	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)
rs58549877	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
122446, ss77337841, ss81352708, ss85088701, ss89529637, ss112610678, ss114406131, ss118385660, ss167693477, ss168945832, ss170870308, ss198962387, ss208520948, ss254846136, ss281635712, ss286666565, ss291555302, ss1397651755, ss1642291396	NC_000013.9:23137824:A:C	NC_000013.11:23665685:A:C	(self)
60311870, 33494712, 23715559, 3216734, 14943176, 35572445, 12860911, 15595177, 31596173, 8410552, 67119150, 33494712, 7429519, ss226075931, ss236173337, ss242684503, ss563545221, ss659138935, ss990185463, ss1078931977, ss1347469519, ss1427125378, ss1576667582, ss1629876682, ss1672870715, ss1807522170, ss1933553247, ss1967732158, ss2027530740, ss2155894198, ss2628252651, ss2700265348, ss2917531730, ss3010709898, ss3350361107, ss3677977311, ss3739576046, ss3751227035, ss3787401268, ss3792475422, ss3797359115, ss3833444013, ss3840297578, ss3879579193, ss3928395051, ss5209149843, ss5409569853, ss5510905263, ss5654387371, ss5839212006, ss5945792764	NC_000013.10:24239824:A:C	NC_000013.11:23665685:A:C	(self)
79224944, 425345383, 946473, 94620730, 155296703, 12874756825, ss2194823427, ss3027579693, ss3649985779, ss3694912292, ss3816558085, ss3845781949, ss4939751045, ss5293073691, ss5487504269, ss5591699009, ss5760783626, ss5813942906, ss5850644182, ss5924345266	NC_000013.11:23665685:A:C	NC_000013.11:23665685:A:C	(self)
ss11065147, ss13167363	NT_009799.12:5219824:A:C	NC_000013.11:23665685:A:C	(self)
ss19265408, ss19961924, ss21135734	NT_024524.13:5219824:A:C	NC_000013.11:23665685:A:C	(self)
ss2094992, ss6227730, ss103102079, ss133480589, ss154522919, ss161581355	NT_024524.14:5219824:A:C	NC_000013.11:23665685:A:C	(self)
35572445, ss3928395051	NC_000013.10:24239824:A:G	NC_000013.11:23665685:A: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 rs1575667

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
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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

rs1575667