Name: rs7216307
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.

rs7216307

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:44336113 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.447429 (118430/264690, TOPMED)
T=0.349483 (67033/191806, ALFA)
T=0.427682 (59855/139952, GnomAD) (+ 19 more)
C=0.14592 (4123/28256, 14KJPN)
C=0.14280 (2393/16758, 8.3KJPN)
C=0.4155 (2661/6404, 1000G_30x)
C=0.4073 (2040/5008, 1000G)
T=0.3873 (1735/4480, Estonian)
T=0.3290 (1268/3854, ALSPAC)
T=0.3293 (1221/3708, TWINSUK)
C=0.1014 (297/2930, KOREAN)
C=0.3858 (804/2084, HGDP_Stanford)
C=0.4264 (805/1888, HapMap)
C=0.0939 (172/1832, Korea1K)
T=0.311 (310/998, GoNL)
T=0.315 (189/600, NorthernSweden)
C=0.232 (110/474, SGDP_PRJ)
T=0.417 (90/216, Qatari)
C=0.070 (15/214, Vietnamese)
T=0.21 (18/84, Ancient Sardinia)
C=0.17 (8/48, Siberian)
T=0.35 (14/40, GENOME_DK)

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	191806	C=0.650517	A=0.000000, T=0.349483
European	Sub	165318	C=0.675383	A=0.000000, T=0.324617
African	Sub	7508	C=0.5216	A=0.0000, T=0.4784
African Others	Sub	260	C=0.488	A=0.000, T=0.512
African American	Sub	7248	C=0.5228	A=0.0000, T=0.4772
Asian	Sub	592	C=0.090	A=0.000, T=0.910
East Asian	Sub	470	C=0.091	A=0.000, T=0.909
Other Asian	Sub	122	C=0.082	A=0.000, T=0.918
Latin American 1	Sub	728	C=0.625	A=0.000, T=0.375
Latin American 2	Sub	6396	C=0.4647	A=0.0000, T=0.5353
South Asian	Sub	4964	C=0.3944	A=0.0000, T=0.6056
Other	Sub	6300	C=0.5978	A=0.0000, T=0.4022

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=0.552571	T=0.447429
Allele Frequency Aggregator	Total	Global	191806	C=0.650517	A=0.000000, T=0.349483
Allele Frequency Aggregator	European	Sub	165318	C=0.675383	A=0.000000, T=0.324617
Allele Frequency Aggregator	African	Sub	7508	C=0.5216	A=0.0000, T=0.4784
Allele Frequency Aggregator	Latin American 2	Sub	6396	C=0.4647	A=0.0000, T=0.5353
Allele Frequency Aggregator	Other	Sub	6300	C=0.5978	A=0.0000, T=0.4022
Allele Frequency Aggregator	South Asian	Sub	4964	C=0.3944	A=0.0000, T=0.6056
Allele Frequency Aggregator	Latin American 1	Sub	728	C=0.625	A=0.000, T=0.375
Allele Frequency Aggregator	Asian	Sub	592	C=0.090	A=0.000, T=0.910
gnomAD - Genomes	Global	Study-wide	139952	C=0.572318	T=0.427682
gnomAD - Genomes	European	Sub	75814	C=0.65107	T=0.34893
gnomAD - Genomes	African	Sub	41924	C=0.47794	T=0.52206
gnomAD - Genomes	American	Sub	13626	C=0.51321	T=0.48679
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.6961	T=0.3039
gnomAD - Genomes	East Asian	Sub	3126	C=0.0720	T=0.9280
gnomAD - Genomes	Other	Sub	2138	C=0.5463	T=0.4537
14KJPN	JAPANESE	Study-wide	28256	C=0.14592	T=0.85408
8.3KJPN	JAPANESE	Study-wide	16758	C=0.14280	T=0.85720
1000Genomes_30x	Global	Study-wide	6404	C=0.4155	T=0.5845
1000Genomes_30x	African	Sub	1786	C=0.4742	T=0.5258
1000Genomes_30x	Europe	Sub	1266	C=0.6461	T=0.3539
1000Genomes_30x	South Asian	Sub	1202	C=0.3536	T=0.6464
1000Genomes_30x	East Asian	Sub	1170	C=0.0701	T=0.9299
1000Genomes_30x	American	Sub	980	C=0.499	T=0.501
1000Genomes	Global	Study-wide	5008	C=0.4073	T=0.5927
1000Genomes	African	Sub	1322	C=0.4788	T=0.5212
1000Genomes	East Asian	Sub	1008	C=0.0744	T=0.9256
1000Genomes	Europe	Sub	1006	C=0.6352	T=0.3648
1000Genomes	South Asian	Sub	978	C=0.358	T=0.642
1000Genomes	American	Sub	694	C=0.494	T=0.506
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.6127	T=0.3873
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6710	T=0.3290
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6707	T=0.3293
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.1014	T=0.8986
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.3858	T=0.6142
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.117	T=0.883
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.440	T=0.560
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.629	T=0.371
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.650	T=0.350
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.417	T=0.583
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.134	T=0.866
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.12	T=0.88
HapMap	Global	Study-wide	1888	C=0.4264	T=0.5736
HapMap	American	Sub	768	C=0.421	T=0.579
HapMap	African	Sub	690	C=0.487	T=0.513
HapMap	Asian	Sub	254	C=0.126	T=0.874
HapMap	Europe	Sub	176	C=0.648	T=0.352
Korean Genome Project	KOREAN	Study-wide	1832	C=0.0939	T=0.9061
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.689	T=0.311
Northern Sweden	ACPOP	Study-wide	600	C=0.685	T=0.315
SGDP_PRJ	Global	Study-wide	474	C=0.232	T=0.768
Qatari	Global	Study-wide	216	C=0.583	T=0.417
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.070	T=0.930
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	84	C=0.79	T=0.21
Siberian	Global	Study-wide	48	C=0.17	T=0.83
The Danish reference pan genome	Danish	Study-wide	40	C=0.65	T=0.35

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 17	NC_000017.11:g.44336113C>A
GRCh38.p14 chr 17	NC_000017.11:g.44336113C>T
GRCh37.p13 chr 17	NC_000017.10:g.42413481C>A
GRCh37.p13 chr 17	NC_000017.10:g.42413481C>T

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	C=	A	T
GRCh38.p14 chr 17	NC_000017.11:g.44336113=	NC_000017.11:g.44336113C>A	NC_000017.11:g.44336113C>T
GRCh37.p13 chr 17	NC_000017.10:g.42413481=	NC_000017.10:g.42413481C>A	NC_000017.10:g.42413481C>T

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#.

121 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10862993	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss19361439	Feb 27, 2004 (120)
3	PERLEGEN	ss23605334	Sep 20, 2004 (123)
4	ABI	ss44035307	Mar 13, 2006 (126)
5	ILLUMINA	ss66564972	Dec 01, 2006 (127)
6	ILLUMINA	ss67557184	Dec 01, 2006 (127)
7	ILLUMINA	ss67933678	Dec 01, 2006 (127)
8	ILLUMINA	ss70916845	May 25, 2008 (130)
9	ILLUMINA	ss71515750	May 18, 2007 (127)
10	ILLUMINA	ss75805643	Dec 06, 2007 (129)
11	ILLUMINA	ss79250426	Dec 15, 2007 (130)
12	KRIBB_YJKIM	ss84639500	Dec 15, 2007 (130)
13	BCMHGSC_JDW	ss90592644	Mar 24, 2008 (129)
14	BGI	ss106507971	Feb 05, 2009 (130)
15	HGSV	ss107790336	Feb 05, 2009 (130)
16	1000GENOMES	ss113554036	Jan 25, 2009 (130)
17	ILLUMINA	ss122717386	Dec 01, 2009 (131)
18	ENSEMBL	ss137078072	Dec 01, 2009 (131)
19	ILLUMINA	ss154413301	Dec 01, 2009 (131)
20	GMI	ss158045955	Dec 01, 2009 (131)
21	ILLUMINA	ss159588394	Dec 01, 2009 (131)
22	ILLUMINA	ss160861369	Dec 01, 2009 (131)
23	ENSEMBL	ss161831328	Dec 01, 2009 (131)
24	COMPLETE_GENOMICS	ss169661570	Jul 04, 2010 (132)
25	ILLUMINA	ss172263786	Jul 04, 2010 (132)
26	ILLUMINA	ss174294438	Jul 04, 2010 (132)
27	BUSHMAN	ss202532215	Jul 04, 2010 (132)
28	ILLUMINA	ss209092161	Jul 04, 2010 (132)
29	1000GENOMES	ss227553150	Jul 14, 2010 (132)
30	1000GENOMES	ss237247033	Jul 15, 2010 (132)
31	1000GENOMES	ss243544620	Jul 15, 2010 (132)
32	ILLUMINA	ss244308632	Jul 04, 2010 (132)
33	BL	ss255646500	May 09, 2011 (134)
34	GMI	ss282770395	May 04, 2012 (137)
35	GMI	ss287182722	Apr 25, 2013 (138)
36	PJP	ss292053678	May 09, 2011 (134)
37	ILLUMINA	ss481509472	May 04, 2012 (137)
38	ILLUMINA	ss481538040	May 04, 2012 (137)
39	ILLUMINA	ss482513489	Sep 08, 2015 (146)
40	ILLUMINA	ss485549771	May 04, 2012 (137)
41	ILLUMINA	ss537451668	Sep 08, 2015 (146)
42	TISHKOFF	ss565280441	Apr 25, 2013 (138)
43	SSMP	ss661083119	Apr 25, 2013 (138)
44	ILLUMINA	ss778968655	Sep 08, 2015 (146)
45	ILLUMINA	ss783220448	Sep 08, 2015 (146)
46	ILLUMINA	ss784174908	Sep 08, 2015 (146)
47	ILLUMINA	ss825580944	Apr 01, 2015 (144)
48	ILLUMINA	ss832480674	Sep 08, 2015 (146)
49	ILLUMINA	ss833099429	Jul 13, 2019 (153)
50	ILLUMINA	ss834430676	Sep 08, 2015 (146)
51	EVA-GONL	ss993119603	Aug 21, 2014 (142)
52	JMKIDD_LAB	ss1081066531	Aug 21, 2014 (142)
53	1000GENOMES	ss1358704713	Aug 21, 2014 (142)
54	DDI	ss1428036907	Apr 01, 2015 (144)
55	EVA_GENOME_DK	ss1578161448	Apr 01, 2015 (144)
56	EVA_UK10K_ALSPAC	ss1635676964	Apr 01, 2015 (144)
57	EVA_UK10K_TWINSUK	ss1678670997	Apr 01, 2015 (144)
58	EVA_DECODE	ss1697162958	Apr 01, 2015 (144)
59	EVA_SVP	ss1713583323	Apr 01, 2015 (144)
60	ILLUMINA	ss1752226774	Sep 08, 2015 (146)
61	HAMMER_LAB	ss1808788309	Sep 08, 2015 (146)
62	WEILL_CORNELL_DGM	ss1936580098	Feb 12, 2016 (147)
63	GENOMED	ss1968392007	Jul 19, 2016 (147)
64	JJLAB	ss2029066612	Sep 14, 2016 (149)
65	ILLUMINA	ss2095075343	Dec 20, 2016 (150)
66	USC_VALOUEV	ss2157538375	Dec 20, 2016 (150)
67	HUMAN_LONGEVITY	ss2216942663	Dec 20, 2016 (150)
68	SYSTEMSBIOZJU	ss2629029363	Nov 08, 2017 (151)
69	ILLUMINA	ss2633398272	Nov 08, 2017 (151)
70	GRF	ss2702100774	Nov 08, 2017 (151)
71	GNOMAD	ss2950017676	Nov 08, 2017 (151)
72	SWEGEN	ss3015555356	Nov 08, 2017 (151)
73	BIOINF_KMB_FNS_UNIBA	ss3028353571	Nov 08, 2017 (151)
74	CSHL	ss3351751703	Nov 08, 2017 (151)
75	ILLUMINA	ss3627672911	Oct 12, 2018 (152)
76	ILLUMINA	ss3631379268	Oct 12, 2018 (152)
77	ILLUMINA	ss3633141931	Oct 12, 2018 (152)
78	ILLUMINA	ss3633849492	Oct 12, 2018 (152)
79	ILLUMINA	ss3634676219	Oct 12, 2018 (152)
80	ILLUMINA	ss3635537240	Oct 12, 2018 (152)
81	ILLUMINA	ss3636365830	Oct 12, 2018 (152)
82	ILLUMINA	ss3637288790	Oct 12, 2018 (152)
83	ILLUMINA	ss3638162369	Oct 12, 2018 (152)
84	ILLUMINA	ss3639090264	Oct 12, 2018 (152)
85	ILLUMINA	ss3639552163	Oct 12, 2018 (152)
86	ILLUMINA	ss3640383531	Oct 12, 2018 (152)
87	ILLUMINA	ss3641081072	Oct 12, 2018 (152)
88	ILLUMINA	ss3641376564	Oct 12, 2018 (152)
89	ILLUMINA	ss3643140707	Oct 12, 2018 (152)
90	ILLUMINA	ss3652198924	Oct 12, 2018 (152)
91	EGCUT_WGS	ss3682441169	Jul 13, 2019 (153)
92	EVA_DECODE	ss3700490903	Jul 13, 2019 (153)
93	ACPOP	ss3742035846	Jul 13, 2019 (153)
94	ILLUMINA	ss3744976513	Jul 13, 2019 (153)
95	EVA	ss3754681410	Jul 13, 2019 (153)
96	ILLUMINA	ss3772474383	Jul 13, 2019 (153)
97	KHV_HUMAN_GENOMES	ss3819950599	Jul 13, 2019 (153)
98	EVA	ss3834873394	Apr 27, 2020 (154)
99	EVA	ss3841046709	Apr 27, 2020 (154)
100	EVA	ss3846543657	Apr 27, 2020 (154)
101	HGDP	ss3847564354	Apr 27, 2020 (154)
102	SGDP_PRJ	ss3885774575	Apr 27, 2020 (154)
103	KRGDB	ss3935467993	Apr 27, 2020 (154)
104	KOGIC	ss3978872619	Apr 27, 2020 (154)
105	EVA	ss3985791749	Apr 27, 2021 (155)
106	EVA	ss4017767614	Apr 27, 2021 (155)
107	TOPMED	ss5036429117	Apr 27, 2021 (155)
108	TOMMO_GENOMICS	ss5222476623	Apr 27, 2021 (155)
109	1000G_HIGH_COVERAGE	ss5303177960	Oct 16, 2022 (156)
110	EVA	ss5315887437	Oct 16, 2022 (156)
111	EVA	ss5427675625	Oct 16, 2022 (156)
112	HUGCELL_USP	ss5496228838	Oct 16, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5606919093	Oct 16, 2022 (156)
114	SANFORD_IMAGENETICS	ss5660127634	Oct 16, 2022 (156)
115	TOMMO_GENOMICS	ss5778707877	Oct 16, 2022 (156)
116	EVA	ss5799975907	Oct 16, 2022 (156)
117	YY_MCH	ss5816552998	Oct 16, 2022 (156)
118	EVA	ss5834000554	Oct 16, 2022 (156)
119	EVA	ss5851813047	Oct 16, 2022 (156)
120	EVA	ss5914007772	Oct 16, 2022 (156)
121	EVA	ss5951520614	Oct 16, 2022 (156)
122	1000Genomes	NC_000017.10 - 42413481	Oct 12, 2018 (152)
123	1000Genomes_30x	NC_000017.11 - 44336113	Oct 16, 2022 (156)
124	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 42413481	Oct 12, 2018 (152)
125	Genetic variation in the Estonian population	NC_000017.10 - 42413481	Oct 12, 2018 (152)
126	The Danish reference pan genome	NC_000017.10 - 42413481	Apr 27, 2020 (154)
127	gnomAD - Genomes	NC_000017.11 - 44336113	Apr 27, 2021 (155)
128	Genome of the Netherlands Release 5	NC_000017.10 - 42413481	Apr 27, 2020 (154)
129	HGDP-CEPH-db Supplement 1	NC_000017.9 - 39769007	Apr 27, 2020 (154)
130	HapMap	NC_000017.11 - 44336113	Apr 27, 2020 (154)
131	KOREAN population from KRGDB	NC_000017.10 - 42413481	Apr 27, 2020 (154)
132	Korean Genome Project	NC_000017.11 - 44336113	Apr 27, 2020 (154)
133	Northern Sweden	NC_000017.10 - 42413481	Jul 13, 2019 (153)
134	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000017.10 - 42413481	Apr 27, 2021 (155)
135	Qatari	NC_000017.10 - 42413481	Apr 27, 2020 (154)
136	SGDP_PRJ	NC_000017.10 - 42413481	Apr 27, 2020 (154)
137	Siberian	NC_000017.10 - 42413481	Apr 27, 2020 (154)
138	8.3KJPN	NC_000017.10 - 42413481	Apr 27, 2021 (155)
139	14KJPN	NC_000017.11 - 44336113	Oct 16, 2022 (156)
140	TopMed	NC_000017.11 - 44336113	Apr 27, 2021 (155)
141	UK 10K study - Twins	NC_000017.10 - 42413481	Oct 12, 2018 (152)
142	A Vietnamese Genetic Variation Database	NC_000017.10 - 42413481	Jul 13, 2019 (153)
143	ALFA	NC_000017.11 - 44336113	Apr 27, 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)
rs59847034	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5662358028	NC_000017.11:44336112:C:A	NC_000017.11:44336112:C:A	(self)
242246, ss90592644, ss113554036, ss169661570, ss202532215, ss255646500, ss282770395, ss287182722, ss292053678, ss481509472, ss825580944, ss1697162958, ss1713583323, ss3639090264, ss3639552163, ss3643140707, ss3847564354	NC_000017.9:39769006:C:T	NC_000017.11:44336112:C:T	(self)
71948301, 39875489, 28179417, 4363679, 17771006, 42645387, 15320711, 1017676, 18622020, 37791555, 10054729, 80445930, 39875489, 8822742, ss227553150, ss237247033, ss243544620, ss481538040, ss482513489, ss485549771, ss537451668, ss565280441, ss661083119, ss778968655, ss783220448, ss784174908, ss832480674, ss833099429, ss834430676, ss993119603, ss1081066531, ss1358704713, ss1428036907, ss1578161448, ss1635676964, ss1678670997, ss1752226774, ss1808788309, ss1936580098, ss1968392007, ss2029066612, ss2095075343, ss2157538375, ss2629029363, ss2633398272, ss2702100774, ss2950017676, ss3015555356, ss3351751703, ss3627672911, ss3631379268, ss3633141931, ss3633849492, ss3634676219, ss3635537240, ss3636365830, ss3637288790, ss3638162369, ss3640383531, ss3641081072, ss3641376564, ss3652198924, ss3682441169, ss3742035846, ss3744976513, ss3754681410, ss3772474383, ss3834873394, ss3841046709, ss3885774575, ss3935467993, ss3985791749, ss4017767614, ss5222476623, ss5315887437, ss5427675625, ss5660127634, ss5799975907, ss5834000554, ss5951520614	NC_000017.10:42413480:C:T	NC_000017.11:44336112:C:T	(self)
94445028, 507623650, 1490015, 35250620, 112544981, 251974779, 5662358028, ss2216942663, ss3028353571, ss3700490903, ss3819950599, ss3846543657, ss3978872619, ss5036429117, ss5303177960, ss5496228838, ss5606919093, ss5778707877, ss5816552998, ss5851813047, ss5914007772	NC_000017.11:44336112:C:T	NC_000017.11:44336112:C:T	(self)
ss10862993	NT_010748.12:1067285:C:T	NC_000017.11:44336112:C:T	(self)
ss19361439	NT_010783.14:1067285:C:T	NC_000017.11:44336112:C:T	(self)
ss23605334, ss44035307, ss66564972, ss67557184, ss67933678, ss70916845, ss71515750, ss75805643, ss79250426, ss84639500, ss106507971, ss107790336, ss122717386, ss137078072, ss154413301, ss158045955, ss159588394, ss160861369, ss161831328, ss172263786, ss174294438, ss209092161, ss244308632	NT_010783.15:7687632:C:T	NC_000017.11:44336112: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 rs7216307

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

rs7216307