Name: rs724291
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.

rs724291

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:33759525 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.407386 (107831/264690, TOPMED)
T=0.485691 (82006/168844, ALFA)
C=0.414583 (58093/140124, GnomAD) (+ 16 more)
C=0.3562 (2281/6404, 1000G_30x)
C=0.3580 (1793/5008, 1000G)
T=0.4542 (2035/4480, Estonian)
T=0.4541 (1750/3854, ALSPAC)
T=0.4436 (1645/3708, TWINSUK)
C=0.4126 (1209/2930, KOREAN)
C=0.3853 (803/2084, HGDP_Stanford)
C=0.3317 (627/1890, HapMap)
T=0.423 (422/998, GoNL)
T=0.458 (275/600, NorthernSweden)
T=0.365 (122/334, SGDP_PRJ)
C=0.264 (57/216, Qatari)
C=0.229 (49/214, Vietnamese)
T=0.44 (34/78, Ancient Sardinia)
T=0.30 (12/40, GENOME_DK)
T=0.31 (11/36, Siberian)

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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	168844	T=0.485691	A=0.000000, C=0.514309
European	Sub	148034	T=0.462907	A=0.000000, C=0.537093
African	Sub	6422	T=0.8572	A=0.0000, C=0.1428
African Others	Sub	234	T=0.936	A=0.000, C=0.064
African American	Sub	6188	T=0.8542	A=0.0000, C=0.1458
Asian	Sub	502	T=0.655	A=0.000, C=0.345
East Asian	Sub	400	T=0.650	A=0.000, C=0.350
Other Asian	Sub	102	T=0.676	A=0.000, C=0.324
Latin American 1	Sub	666	T=0.602	A=0.000, C=0.398
Latin American 2	Sub	3158	T=0.5722	A=0.0000, C=0.4278
South Asian	Sub	4954	T=0.5692	A=0.0000, C=0.4308
Other	Sub	5108	T=0.5125	A=0.0000, C=0.4875

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=0.592614	C=0.407386
Allele Frequency Aggregator	Total	Global	168844	T=0.485691	A=0.000000, C=0.514309
Allele Frequency Aggregator	European	Sub	148034	T=0.462907	A=0.000000, C=0.537093
Allele Frequency Aggregator	African	Sub	6422	T=0.8572	A=0.0000, C=0.1428
Allele Frequency Aggregator	Other	Sub	5108	T=0.5125	A=0.0000, C=0.4875
Allele Frequency Aggregator	South Asian	Sub	4954	T=0.5692	A=0.0000, C=0.4308
Allele Frequency Aggregator	Latin American 2	Sub	3158	T=0.5722	A=0.0000, C=0.4278
Allele Frequency Aggregator	Latin American 1	Sub	666	T=0.602	A=0.000, C=0.398
Allele Frequency Aggregator	Asian	Sub	502	T=0.655	A=0.000, C=0.345
gnomAD - Genomes	Global	Study-wide	140124	T=0.585417	C=0.414583
gnomAD - Genomes	European	Sub	75872	T=0.45855	C=0.54145
gnomAD - Genomes	African	Sub	42000	T=0.81357	C=0.18643
gnomAD - Genomes	American	Sub	13658	T=0.57798	C=0.42202
gnomAD - Genomes	Ashkenazi Jewish	Sub	3316	T=0.5947	C=0.4053
gnomAD - Genomes	East Asian	Sub	3124	T=0.6274	C=0.3726
gnomAD - Genomes	Other	Sub	2154	T=0.5775	C=0.4225
1000Genomes_30x	Global	Study-wide	6404	T=0.6438	C=0.3562
1000Genomes_30x	African	Sub	1786	T=0.8611	C=0.1389
1000Genomes_30x	Europe	Sub	1266	T=0.4850	C=0.5150
1000Genomes_30x	South Asian	Sub	1202	T=0.5932	C=0.4068
1000Genomes_30x	East Asian	Sub	1170	T=0.6325	C=0.3675
1000Genomes_30x	American	Sub	980	T=0.529	C=0.471
1000Genomes	Global	Study-wide	5008	T=0.6420	C=0.3580
1000Genomes	African	Sub	1322	T=0.8623	C=0.1377
1000Genomes	East Asian	Sub	1008	T=0.6270	C=0.3730
1000Genomes	Europe	Sub	1006	T=0.4891	C=0.5109
1000Genomes	South Asian	Sub	978	T=0.589	C=0.411
1000Genomes	American	Sub	694	T=0.540	C=0.460
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4542	C=0.5458
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4541	C=0.5459
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4436	C=0.5564
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.5857	A=0.0017, C=0.4126
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6147	C=0.3853
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.640	C=0.360
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.585	C=0.415
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.571	C=0.429
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.497	C=0.503
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.897	C=0.103
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.569	C=0.431
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.54	C=0.46
HapMap	Global	Study-wide	1890	T=0.6683	C=0.3317
HapMap	American	Sub	770	T=0.565	C=0.435
HapMap	African	Sub	690	T=0.881	C=0.119
HapMap	Asian	Sub	254	T=0.535	C=0.465
HapMap	Europe	Sub	176	T=0.477	C=0.523
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.423	C=0.577
Northern Sweden	ACPOP	Study-wide	600	T=0.458	C=0.542
SGDP_PRJ	Global	Study-wide	334	T=0.365	C=0.635
Qatari	Global	Study-wide	216	T=0.736	C=0.264
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.771	C=0.229
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	78	T=0.44	C=0.56
The Danish reference pan genome	Danish	Study-wide	40	T=0.30	C=0.70
Siberian	Global	Study-wide	36	T=0.31	C=0.69

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 7	NC_000007.14:g.33759525T>A
GRCh38.p14 chr 7	NC_000007.14:g.33759525T>C
GRCh37.p13 chr 7	NC_000007.13:g.33799137T>A
GRCh37.p13 chr 7	NC_000007.13:g.33799137T>C

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
GRCh38.p14 chr 7	NC_000007.14:g.33759525=	NC_000007.14:g.33759525T>A	NC_000007.14:g.33759525T>C
GRCh37.p13 chr 7	NC_000007.13:g.33799137=	NC_000007.13:g.33799137T>A	NC_000007.13:g.33799137T>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#.

125 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss66848	Oct 05, 2000 (86)
2	WI_SSAHASNP	ss6504900	Feb 20, 2003 (111)
3	WUGSC_SSAHASNP	ss14591074	Dec 05, 2003 (120)
4	CSHL-HAPMAP	ss20327080	Feb 27, 2004 (120)
5	SSAHASNP	ss22643321	Apr 05, 2004 (121)
6	SSAHASNP	ss22958683	Apr 05, 2004 (121)
7	PERLEGEN	ss24046329	Sep 20, 2004 (123)
8	ABI	ss44827677	Mar 15, 2006 (126)
9	AFFY	ss66453965	Nov 30, 2006 (127)
10	ILLUMINA	ss66625577	Nov 30, 2006 (127)
11	ILLUMINA	ss67560954	Nov 30, 2006 (127)
12	ILLUMINA	ss67938426	Nov 30, 2006 (127)
13	ILLUMINA	ss70918801	May 25, 2008 (130)
14	ILLUMINA	ss71518136	May 17, 2007 (127)
15	ILLUMINA	ss75456688	Dec 06, 2007 (129)
16	AFFY	ss76246732	Dec 08, 2007 (130)
17	ILLUMINA	ss79251612	Dec 15, 2007 (130)
18	KRIBB_YJKIM	ss83534027	Dec 15, 2007 (130)
19	HGSV	ss84162352	Dec 15, 2007 (130)
20	BCMHGSC_JDW	ss93657643	Mar 24, 2008 (129)
21	HUMANGENOME_JCVI	ss98144659	Feb 06, 2009 (130)
22	BGI	ss104415869	Dec 01, 2009 (131)
23	1000GENOMES	ss111790439	Jan 25, 2009 (130)
24	ILLUMINA-UK	ss116020665	Feb 14, 2009 (130)
25	ILLUMINA	ss120243076	Dec 01, 2009 (131)
26	ILLUMINA	ss122724463	Dec 01, 2009 (131)
27	ENSEMBL	ss142828844	Dec 01, 2009 (131)
28	ENSEMBL	ss143656781	Dec 01, 2009 (131)
29	ILLUMINA	ss154415357	Dec 01, 2009 (131)
30	ILLUMINA	ss159590439	Dec 01, 2009 (131)
31	ILLUMINA	ss160864741	Dec 01, 2009 (131)
32	COMPLETE_GENOMICS	ss162202175	Jul 04, 2010 (132)
33	COMPLETE_GENOMICS	ss166401447	Jul 04, 2010 (132)
34	ILLUMINA	ss172268916	Jul 04, 2010 (132)
35	AFFY	ss172961825	Jul 04, 2010 (132)
36	ILLUMINA	ss174306399	Jul 04, 2010 (132)
37	BUSHMAN	ss203165654	Jul 04, 2010 (132)
38	BCM-HGSC-SUB	ss208227252	Jul 04, 2010 (132)
39	1000GENOMES	ss223004275	Jul 14, 2010 (132)
40	1000GENOMES	ss233921099	Jul 15, 2010 (132)
41	1000GENOMES	ss240886849	Jul 15, 2010 (132)
42	ILLUMINA	ss244257689	Jul 04, 2010 (132)
43	BL	ss254176236	May 09, 2011 (134)
44	GMI	ss279253954	May 04, 2012 (137)
45	GMI	ss285603449	Apr 25, 2013 (138)
46	PJP	ss294044679	May 09, 2011 (134)
47	ILLUMINA	ss481548941	May 04, 2012 (137)
48	ILLUMINA	ss482523537	Sep 08, 2015 (146)
49	ILLUMINA	ss537455489	Sep 08, 2015 (146)
50	TISHKOFF	ss559917708	Apr 25, 2013 (138)
51	SSMP	ss654273003	Apr 25, 2013 (138)
52	ILLUMINA	ss825582130	Apr 01, 2015 (144)
53	ILLUMINA	ss832483415	Apr 01, 2015 (144)
54	ILLUMINA	ss833101471	Aug 21, 2014 (142)
55	ILLUMINA	ss833692299	Aug 21, 2014 (142)
56	EVA-GONL	ss984133545	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1074501379	Aug 21, 2014 (142)
58	1000GENOMES	ss1324595707	Aug 21, 2014 (142)
59	DDI	ss1431081156	Apr 01, 2015 (144)
60	EVA_GENOME_DK	ss1582143843	Apr 01, 2015 (144)
61	EVA_DECODE	ss1593704984	Apr 01, 2015 (144)
62	EVA_UK10K_ALSPAC	ss1617928377	Apr 01, 2015 (144)
63	EVA_UK10K_TWINSUK	ss1660922410	Apr 01, 2015 (144)
64	EVA_SVP	ss1712945526	Apr 01, 2015 (144)
65	ILLUMINA	ss1752683131	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1927377564	Feb 12, 2016 (147)
67	GENOMED	ss1970667440	Jul 19, 2016 (147)
68	JJLAB	ss2024368842	Sep 14, 2016 (149)
69	USC_VALOUEV	ss2152564272	Dec 20, 2016 (150)
70	HUMAN_LONGEVITY	ss2293021345	Dec 20, 2016 (150)
71	SYSTEMSBIOZJU	ss2626672306	Nov 08, 2017 (151)
72	ILLUMINA	ss2634590362	Nov 08, 2017 (151)
73	GRF	ss2708223467	Nov 08, 2017 (151)
74	GNOMAD	ss2851636547	Nov 08, 2017 (151)
75	SWEGEN	ss3000898198	Nov 08, 2017 (151)
76	BIOINF_KMB_FNS_UNIBA	ss3025978832	Nov 08, 2017 (151)
77	CSHL	ss3347519550	Nov 08, 2017 (151)
78	ILLUMINA	ss3629789477	Oct 12, 2018 (152)
79	ILLUMINA	ss3633459032	Oct 12, 2018 (152)
80	ILLUMINA	ss3634183738	Oct 12, 2018 (152)
81	ILLUMINA	ss3635116024	Oct 12, 2018 (152)
82	ILLUMINA	ss3635863659	Oct 12, 2018 (152)
83	ILLUMINA	ss3636847624	Oct 12, 2018 (152)
84	ILLUMINA	ss3637616610	Oct 12, 2018 (152)
85	ILLUMINA	ss3638690459	Oct 12, 2018 (152)
86	ILLUMINA	ss3639347898	Oct 12, 2018 (152)
87	ILLUMINA	ss3639701750	Oct 12, 2018 (152)
88	ILLUMINA	ss3640823320	Oct 12, 2018 (152)
89	ILLUMINA	ss3643627080	Oct 12, 2018 (152)
90	URBANLAB	ss3648600232	Oct 12, 2018 (152)
91	EGCUT_WGS	ss3668824798	Jul 13, 2019 (153)
92	EVA_DECODE	ss3719430278	Jul 13, 2019 (153)
93	ACPOP	ss3734509704	Jul 13, 2019 (153)
94	ILLUMINA	ss3745415975	Jul 13, 2019 (153)
95	EVA	ss3766395070	Jul 13, 2019 (153)
96	ILLUMINA	ss3772909058	Jul 13, 2019 (153)
97	PACBIO	ss3785779251	Jul 13, 2019 (153)
98	PACBIO	ss3791087053	Jul 13, 2019 (153)
99	PACBIO	ss3795966851	Jul 13, 2019 (153)
100	KHV_HUMAN_GENOMES	ss3809561110	Jul 13, 2019 (153)
101	EVA	ss3830503651	Apr 26, 2020 (154)
102	EVA	ss3838740138	Apr 26, 2020 (154)
103	EVA	ss3844191728	Apr 26, 2020 (154)
104	HGDP	ss3847872665	Apr 26, 2020 (154)
105	SGDP_PRJ	ss3866987812	Apr 26, 2020 (154)
106	KRGDB	ss3914035910	Apr 26, 2020 (154)
107	EVA	ss3985288603	Apr 26, 2021 (155)
108	EVA	ss4017329729	Apr 26, 2021 (155)
109	TOPMED	ss4741353325	Apr 26, 2021 (155)
110	TOMMO_GENOMICS	ss5182552764	Apr 26, 2021 (155)
111	TOMMO_GENOMICS	ss5182552765	Apr 26, 2021 (155)
112	1000G_HIGH_COVERAGE	ss5272411418	Oct 14, 2022 (156)
113	EVA	ss5315238827	Oct 14, 2022 (156)
114	EVA	ss5372709018	Oct 14, 2022 (156)
115	HUGCELL_USP	ss5469637448	Oct 14, 2022 (156)
116	1000G_HIGH_COVERAGE	ss5560344210	Oct 14, 2022 (156)
117	SANFORD_IMAGENETICS	ss5642681479	Oct 14, 2022 (156)
118	TOMMO_GENOMICS	ss5722215529	Oct 14, 2022 (156)
119	TOMMO_GENOMICS	ss5722215530	Oct 14, 2022 (156)
120	EVA	ss5799721152	Oct 14, 2022 (156)
121	YY_MCH	ss5808483015	Oct 14, 2022 (156)
122	EVA	ss5822637892	Oct 14, 2022 (156)
123	EVA	ss5855837024	Oct 14, 2022 (156)
124	EVA	ss5858374250	Oct 14, 2022 (156)
125	EVA	ss5971888263	Oct 14, 2022 (156)
126	1000Genomes	NC_000007.13 - 33799137	Oct 12, 2018 (152)
127	1000Genomes_30x	NC_000007.14 - 33759525	Oct 14, 2022 (156)
128	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 33799137	Oct 12, 2018 (152)
129	Genetic variation in the Estonian population	NC_000007.13 - 33799137	Oct 12, 2018 (152)
130	The Danish reference pan genome	NC_000007.13 - 33799137	Apr 26, 2020 (154)
131	gnomAD - Genomes	NC_000007.14 - 33759525	Apr 26, 2021 (155)
132	Genome of the Netherlands Release 5	NC_000007.13 - 33799137	Apr 26, 2020 (154)
133	HGDP-CEPH-db Supplement 1	NC_000007.12 - 33765662	Apr 26, 2020 (154)
134	HapMap	NC_000007.14 - 33759525	Apr 26, 2020 (154)
135	KOREAN population from KRGDB	NC_000007.13 - 33799137	Apr 26, 2020 (154)
136	Northern Sweden	NC_000007.13 - 33799137	Jul 13, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000007.13 - 33799137	Apr 26, 2021 (155)
138	Qatari	NC_000007.13 - 33799137	Apr 26, 2020 (154)
139	SGDP_PRJ	NC_000007.13 - 33799137	Apr 26, 2020 (154)
140	Siberian	NC_000007.13 - 33799137	Apr 26, 2020 (154)
141	8.3KJPN Submission ignored due to conflicting rows: Row 40522071 (NC_000007.13:33799136:T:C 6260/16758) Row 40522072 (NC_000007.13:33799136:T:A 4/16758)	-	Apr 26, 2021 (155)
142	8.3KJPN Submission ignored due to conflicting rows: Row 40522071 (NC_000007.13:33799136:T:C 6260/16758) Row 40522072 (NC_000007.13:33799136:T:A 4/16758)	-	Apr 26, 2021 (155)
143	14KJPN Submission ignored due to conflicting rows: Row 56052633 (NC_000007.14:33759524:T:C 10670/28258) Row 56052634 (NC_000007.14:33759524:T:A 7/28258)	-	Oct 14, 2022 (156)
144	14KJPN Submission ignored due to conflicting rows: Row 56052633 (NC_000007.14:33759524:T:C 10670/28258) Row 56052634 (NC_000007.14:33759524:T:A 7/28258)	-	Oct 14, 2022 (156)
145	TopMed	NC_000007.14 - 33759525	Apr 26, 2021 (155)
146	UK 10K study - Twins	NC_000007.13 - 33799137	Oct 12, 2018 (152)
147	A Vietnamese Genetic Variation Database	NC_000007.13 - 33799137	Jul 13, 2019 (153)
148	ALFA	NC_000007.14 - 33759525	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)
rs10385453	Feb 27, 2004 (120)
rs17170405	Oct 08, 2004 (123)
rs56596272	May 25, 2008 (130)
rs60301308	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
21213304, ss3914035910, ss5182552765	NC_000007.13:33799136:T:A	NC_000007.14:33759524:T:A	(self)
2110040108, ss5722215530	NC_000007.14:33759524:T:A	NC_000007.14:33759524:T:A	(self)
ss84162352, ss3639347898, ss3639701750	NC_000007.11:33572376:T:C	NC_000007.14:33759524:T:C	(self)
550557, ss93657643, ss111790439, ss116020665, ss160864741, ss162202175, ss166401447, ss203165654, ss208227252, ss254176236, ss279253954, ss285603449, ss294044679, ss825582130, ss1593704984, ss1712945526, ss3643627080, ss3847872665	NC_000007.12:33765661:T:C	NC_000007.14:33759524:T:C	(self)
36547046, 20378003, 14563046, 8308782, 9087350, 21213304, 7794569, 514530, 9419494, 19004792, 5080626, 20378003, 4540812, ss223004275, ss233921099, ss240886849, ss481548941, ss482523537, ss537455489, ss559917708, ss654273003, ss832483415, ss833101471, ss833692299, ss984133545, ss1074501379, ss1324595707, ss1431081156, ss1582143843, ss1617928377, ss1660922410, ss1752683131, ss1927377564, ss1970667440, ss2024368842, ss2152564272, ss2626672306, ss2634590362, ss2708223467, ss2851636547, ss3000898198, ss3347519550, ss3629789477, ss3633459032, ss3634183738, ss3635116024, ss3635863659, ss3636847624, ss3637616610, ss3638690459, ss3640823320, ss3668824798, ss3734509704, ss3745415975, ss3766395070, ss3772909058, ss3785779251, ss3791087053, ss3795966851, ss3830503651, ss3838740138, ss3866987812, ss3914035910, ss3985288603, ss4017329729, ss5182552764, ss5315238827, ss5372709018, ss5642681479, ss5799721152, ss5822637892, ss5971888263	NC_000007.13:33799136:T:C	NC_000007.14:33759524:T:C	(self)
47870145, 257673584, 3374402, 578730884, 2110040108, ss2293021345, ss3025978832, ss3648600232, ss3719430278, ss3809561110, ss3844191728, ss4741353325, ss5272411418, ss5469637448, ss5560344210, ss5722215529, ss5808483015, ss5855837024, ss5858374250	NC_000007.14:33759524:T:C	NC_000007.14:33759524:T:C	(self)
ss14591074, ss20327080, ss22643321, ss22958683	NT_007819.14:33092704:T:C	NC_000007.14:33759524:T:C	(self)
ss66848, ss6504900, ss24046329, ss44827677, ss66453965, ss66625577, ss67560954, ss67938426, ss70918801, ss71518136, ss75456688, ss76246732, ss79251612, ss83534027, ss98144659, ss104415869, ss120243076, ss122724463, ss142828844, ss143656781, ss154415357, ss159590439, ss172268916, ss172961825, ss174306399, ss244257689	NT_007819.17:33789136:T:C	NC_000007.14:33759524: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 rs724291

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

rs724291