Name: rs7920472
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.

rs7920472

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:78321109 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.217968 (57694/264690, TOPMED)
T=0.115885 (26078/225034, ALFA)
T=0.207947 (29138/140122, GnomAD) (+ 19 more)
T=0.26802 (21094/78702, PAGE_STUDY)
T=0.04922 (1391/28258, 14KJPN)
T=0.04899 (821/16760, 8.3KJPN)
T=0.1978 (1267/6404, 1000G_30x)
T=0.1909 (956/5008, 1000G)
T=0.0710 (318/4480, Estonian)
T=0.0520 (152/2922, KOREAN)
T=0.1598 (333/2084, HGDP_Stanford)
T=0.2598 (491/1890, HapMap)
T=0.1092 (124/1136, Daghestan)
T=0.099 (99/998, GoNL)
T=0.072 (45/626, Chileans)
T=0.048 (29/600, NorthernSweden)
T=0.269 (58/216, Qatari)
T=0.056 (12/214, Vietnamese)
C=0.388 (62/160, SGDP_PRJ)
T=0.17 (7/40, GENOME_DK)
T=0.33 (12/36, Ancient Sardinia)
C=0.44 (7/16, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124902468 : 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	225034	C=0.884115	T=0.115885
European	Sub	193090	C=0.898296	T=0.101704
African	Sub	8206	C=0.5257	T=0.4743
African Others	Sub	276	C=0.457	T=0.543
African American	Sub	7930	C=0.5281	T=0.4719
Asian	Sub	828	C=0.946	T=0.054
East Asian	Sub	650	C=0.951	T=0.049
Other Asian	Sub	178	C=0.927	T=0.073
Latin American 1	Sub	990	C=0.805	T=0.195
Latin American 2	Sub	9064	C=0.9116	T=0.0884
South Asian	Sub	5060	C=0.9245	T=0.0755
Other	Sub	7796	C=0.8554	T=0.1446

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=0.782032	T=0.217968
Allele Frequency Aggregator	Total	Global	225034	C=0.884115	T=0.115885
Allele Frequency Aggregator	European	Sub	193090	C=0.898296	T=0.101704
Allele Frequency Aggregator	Latin American 2	Sub	9064	C=0.9116	T=0.0884
Allele Frequency Aggregator	African	Sub	8206	C=0.5257	T=0.4743
Allele Frequency Aggregator	Other	Sub	7796	C=0.8554	T=0.1446
Allele Frequency Aggregator	South Asian	Sub	5060	C=0.9245	T=0.0755
Allele Frequency Aggregator	Latin American 1	Sub	990	C=0.805	T=0.195
Allele Frequency Aggregator	Asian	Sub	828	C=0.946	T=0.054
gnomAD - Genomes	Global	Study-wide	140122	C=0.792053	T=0.207947
gnomAD - Genomes	European	Sub	75922	C=0.91288	T=0.08712
gnomAD - Genomes	African	Sub	41936	C=0.53439	T=0.46561
gnomAD - Genomes	American	Sub	13662	C=0.87293	T=0.12707
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.7951	T=0.2049
gnomAD - Genomes	East Asian	Sub	3128	C=0.9530	T=0.0470
gnomAD - Genomes	Other	Sub	2150	C=0.7981	T=0.2019
The PAGE Study	Global	Study-wide	78702	C=0.73198	T=0.26802
The PAGE Study	AfricanAmerican	Sub	32516	C=0.54112	T=0.45888
The PAGE Study	Mexican	Sub	10810	C=0.91027	T=0.08973
The PAGE Study	Asian	Sub	8318	C=0.9395	T=0.0605
The PAGE Study	PuertoRican	Sub	7918	C=0.7727	T=0.2273
The PAGE Study	NativeHawaiian	Sub	4534	C=0.9455	T=0.0545
The PAGE Study	Cuban	Sub	4230	C=0.8163	T=0.1837
The PAGE Study	Dominican	Sub	3828	C=0.7072	T=0.2928
The PAGE Study	CentralAmerican	Sub	2450	C=0.8600	T=0.1400
The PAGE Study	SouthAmerican	Sub	1982	C=0.8996	T=0.1004
The PAGE Study	NativeAmerican	Sub	1260	C=0.8770	T=0.1230
The PAGE Study	SouthAsian	Sub	856	C=0.932	T=0.068
14KJPN	JAPANESE	Study-wide	28258	C=0.95078	T=0.04922
8.3KJPN	JAPANESE	Study-wide	16760	C=0.95101	T=0.04899
1000Genomes_30x	Global	Study-wide	6404	C=0.8022	T=0.1978
1000Genomes_30x	African	Sub	1786	C=0.4776	T=0.5224
1000Genomes_30x	Europe	Sub	1266	C=0.8965	T=0.1035
1000Genomes_30x	South Asian	Sub	1202	C=0.9509	T=0.0491
1000Genomes_30x	East Asian	Sub	1170	C=0.9744	T=0.0256
1000Genomes_30x	American	Sub	980	C=0.884	T=0.116
1000Genomes	Global	Study-wide	5008	C=0.8091	T=0.1909
1000Genomes	African	Sub	1322	C=0.4773	T=0.5227
1000Genomes	East Asian	Sub	1008	C=0.9722	T=0.0278
1000Genomes	Europe	Sub	1006	C=0.8976	T=0.1024
1000Genomes	South Asian	Sub	978	C=0.953	T=0.047
1000Genomes	American	Sub	694	C=0.873	T=0.127
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9290	T=0.0710
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9480	T=0.0520
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.8402	T=0.1598
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.955	T=0.045
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.901	T=0.099
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.791	T=0.209
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.850	T=0.150
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.430	T=0.570
HGDP-CEPH-db Supplement 1	America	Sub	216	C=1.000	T=0.000
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.83	T=0.17
HapMap	Global	Study-wide	1890	C=0.7402	T=0.2598
HapMap	American	Sub	768	C=0.876	T=0.124
HapMap	African	Sub	692	C=0.483	T=0.517
HapMap	Asian	Sub	254	C=0.945	T=0.055
HapMap	Europe	Sub	176	C=0.864	T=0.136
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	C=0.8908	T=0.1092
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.896	T=0.104
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.847	T=0.153
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.910	T=0.090
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.861	T=0.139
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.94	T=0.06
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.86	T=0.14
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.901	T=0.099
Chileans	Chilean	Study-wide	626	C=0.928	T=0.072
Northern Sweden	ACPOP	Study-wide	600	C=0.952	T=0.048
Qatari	Global	Study-wide	216	C=0.731	T=0.269
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.944	T=0.056
SGDP_PRJ	Global	Study-wide	160	C=0.388	T=0.613
The Danish reference pan genome	Danish	Study-wide	40	C=0.82	T=0.17
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	36	C=0.67	T=0.33
Siberian	Global	Study-wide	16	C=0.44	T=0.56

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 10	NC_000010.11:g.78321109C>T
GRCh37.p13 chr 10	NC_000010.10:g.80080866C>T

Gene: LOC124902468, uncharacterized LOC124902468 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124902468 transcript variant X1	XR_007062211.1:n.	N/A	Intron Variant
LOC124902468 transcript variant X2	XR_007062212.1:n.	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	C=	T
GRCh38.p14 chr 10	NC_000010.11:g.78321109=	NC_000010.11:g.78321109C>T
GRCh37.p13 chr 10	NC_000010.10:g.80080866=	NC_000010.10:g.80080866C>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	WI_SSAHASNP	ss12110923	Jul 11, 2003 (116)
2	ILLUMINA	ss66788784	Dec 01, 2006 (127)
3	ILLUMINA	ss67848082	Dec 01, 2006 (127)
4	ILLUMINA	ss68001968	Dec 01, 2006 (127)
5	ILLUMINA	ss70958581	May 24, 2008 (130)
6	ILLUMINA	ss71566531	May 18, 2007 (127)
7	ILLUMINA	ss75766250	Dec 06, 2007 (129)
8	AFFY	ss76621099	Dec 06, 2007 (129)
9	ILLUMINA	ss79274873	Dec 15, 2007 (130)
10	KRIBB_YJKIM	ss84751121	Dec 15, 2007 (130)
11	HGSV	ss85548251	Dec 15, 2007 (130)
12	HGSV	ss85698462	Dec 15, 2007 (130)
13	BGI	ss102893834	Dec 01, 2009 (131)
14	ILLUMINA	ss122863378	Dec 01, 2009 (131)
15	ILLUMINA	ss154456512	Dec 01, 2009 (131)
16	ILLUMINA	ss159631150	Dec 01, 2009 (131)
17	ILLUMINA	ss160929195	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss168609852	Jul 04, 2010 (132)
19	ILLUMINA	ss172369169	Jul 04, 2010 (132)
20	ILLUMINA	ss174619337	Jul 04, 2010 (132)
21	BUSHMAN	ss201745112	Jul 04, 2010 (132)
22	BCM-HGSC-SUB	ss206996840	Jul 04, 2010 (132)
23	1000GENOMES	ss210767081	Jul 14, 2010 (132)
24	1000GENOMES	ss224823023	Jul 14, 2010 (132)
25	1000GENOMES	ss235246718	Jul 15, 2010 (132)
26	1000GENOMES	ss241940107	Jul 15, 2010 (132)
27	GMI	ss280688343	May 04, 2012 (137)
28	PJP	ss290875573	May 09, 2011 (134)
29	ILLUMINA	ss481718752	May 04, 2012 (137)
30	ILLUMINA	ss481750172	May 04, 2012 (137)
31	ILLUMINA	ss482716306	Sep 08, 2015 (146)
32	ILLUMINA	ss485654116	May 04, 2012 (137)
33	ILLUMINA	ss537531230	Sep 08, 2015 (146)
34	TISHKOFF	ss562071230	Apr 25, 2013 (138)
35	SSMP	ss657014788	Apr 25, 2013 (138)
36	ILLUMINA	ss778990831	Sep 08, 2015 (146)
37	ILLUMINA	ss783272616	Sep 08, 2015 (146)
38	ILLUMINA	ss784225795	Sep 08, 2015 (146)
39	ILLUMINA	ss825605391	Jul 19, 2016 (147)
40	ILLUMINA	ss832533668	Sep 08, 2015 (146)
41	ILLUMINA	ss833142037	Jul 13, 2019 (153)
42	ILLUMINA	ss834453083	Sep 08, 2015 (146)
43	EVA-GONL	ss987678881	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1077127062	Aug 21, 2014 (142)
45	1000GENOMES	ss1338162400	Aug 21, 2014 (142)
46	HAMMER_LAB	ss1397586150	Sep 08, 2015 (146)
47	DDI	ss1426375932	Apr 01, 2015 (144)
48	EVA_GENOME_DK	ss1575223883	Apr 01, 2015 (144)
49	EVA_DECODE	ss1597353487	Apr 01, 2015 (144)
50	EVA_SVP	ss1713193548	Apr 01, 2015 (144)
51	ILLUMINA	ss1751981897	Sep 08, 2015 (146)
52	HAMMER_LAB	ss1806470840	Sep 08, 2015 (146)
53	WEILL_CORNELL_DGM	ss1931045239	Feb 12, 2016 (147)
54	ILLUMINA	ss1959276030	Feb 12, 2016 (147)
55	GENOMED	ss1967171390	Jul 19, 2016 (147)
56	JJLAB	ss2026249197	Sep 14, 2016 (149)
57	USC_VALOUEV	ss2154524554	Dec 20, 2016 (150)
58	HUMAN_LONGEVITY	ss2176237736	Dec 20, 2016 (150)
59	SYSTEMSBIOZJU	ss2627593664	Nov 08, 2017 (151)
60	ILLUMINA	ss2632733703	Nov 08, 2017 (151)
61	ILLUMINA	ss2635016368	Nov 08, 2017 (151)
62	GRF	ss2698771939	Nov 08, 2017 (151)
63	ILLUMINA	ss2710714274	Nov 08, 2017 (151)
64	GNOMAD	ss2890817083	Nov 08, 2017 (151)
65	SWEGEN	ss3006773191	Nov 08, 2017 (151)
66	ILLUMINA	ss3021255350	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3026914652	Nov 08, 2017 (151)
68	CSHL	ss3349205303	Nov 08, 2017 (151)
69	ILLUMINA	ss3626485259	Oct 12, 2018 (152)
70	ILLUMINA	ss3630758047	Oct 12, 2018 (152)
71	ILLUMINA	ss3632955817	Oct 12, 2018 (152)
72	ILLUMINA	ss3633653281	Oct 12, 2018 (152)
73	ILLUMINA	ss3634412113	Oct 12, 2018 (152)
74	ILLUMINA	ss3635345650	Oct 12, 2018 (152)
75	ILLUMINA	ss3636095504	Oct 12, 2018 (152)
76	ILLUMINA	ss3637096342	Oct 12, 2018 (152)
77	ILLUMINA	ss3637860333	Oct 12, 2018 (152)
78	ILLUMINA	ss3638946157	Oct 12, 2018 (152)
79	ILLUMINA	ss3639472908	Oct 12, 2018 (152)
80	ILLUMINA	ss3640119455	Oct 12, 2018 (152)
81	ILLUMINA	ss3641003319	Oct 12, 2018 (152)
82	ILLUMINA	ss3641297615	Oct 12, 2018 (152)
83	ILLUMINA	ss3642863071	Oct 12, 2018 (152)
84	ILLUMINA	ss3651611765	Oct 12, 2018 (152)
85	EGCUT_WGS	ss3674190951	Jul 13, 2019 (153)
86	EVA_DECODE	ss3690235827	Jul 13, 2019 (153)
87	ILLUMINA	ss3725171013	Jul 13, 2019 (153)
88	ACPOP	ss3737481403	Jul 13, 2019 (153)
89	ILLUMINA	ss3744713099	Jul 13, 2019 (153)
90	EVA	ss3748323633	Jul 13, 2019 (153)
91	PAGE_CC	ss3771568949	Jul 13, 2019 (153)
92	ILLUMINA	ss3772213492	Jul 13, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3813693144	Jul 13, 2019 (153)
94	EVA	ss3832217233	Apr 26, 2020 (154)
95	EVA	ss3839646511	Apr 26, 2020 (154)
96	EVA	ss3845119569	Apr 26, 2020 (154)
97	HGDP	ss3847392048	Apr 26, 2020 (154)
98	SGDP_PRJ	ss3874582411	Apr 26, 2020 (154)
99	KRGDB	ss3922686763	Apr 26, 2020 (154)
100	EVA	ss3985485983	Apr 26, 2021 (155)
101	EVA	ss4017495160	Apr 26, 2021 (155)
102	TOPMED	ss4858637468	Apr 26, 2021 (155)
103	TOMMO_GENOMICS	ss5198447317	Apr 26, 2021 (155)
104	EVA	ss5237479821	Apr 26, 2021 (155)
105	1000G_HIGH_COVERAGE	ss5284685414	Oct 16, 2022 (156)
106	EVA	ss5315486035	Oct 16, 2022 (156)
107	EVA	ss5394599824	Oct 16, 2022 (156)
108	HUGCELL_USP	ss5480196717	Oct 16, 2022 (156)
109	1000G_HIGH_COVERAGE	ss5578951700	Oct 16, 2022 (156)
110	SANFORD_IMAGENETICS	ss5624252604	Oct 16, 2022 (156)
111	SANFORD_IMAGENETICS	ss5649651828	Oct 16, 2022 (156)
112	TOMMO_GENOMICS	ss5744516569	Oct 16, 2022 (156)
113	EVA	ss5799817796	Oct 16, 2022 (156)
114	YY_MCH	ss5811689128	Oct 16, 2022 (156)
115	EVA	ss5824647055	Oct 16, 2022 (156)
116	EVA	ss5847376023	Oct 16, 2022 (156)
117	EVA	ss5847601834	Oct 16, 2022 (156)
118	EVA	ss5849645463	Oct 16, 2022 (156)
119	EVA	ss5879631426	Oct 16, 2022 (156)
120	EVA	ss5940932245	Oct 16, 2022 (156)
121	EVA	ss5979331584	Oct 16, 2022 (156)
122	1000Genomes	NC_000010.10 - 80080866	Oct 12, 2018 (152)
123	1000Genomes_30x	NC_000010.11 - 78321109	Oct 16, 2022 (156)
124	Chileans	NC_000010.10 - 80080866	Apr 26, 2020 (154)
125	Genome-wide autozygosity in Daghestan	NC_000010.9 - 79750872	Apr 26, 2020 (154)
126	Genetic variation in the Estonian population	NC_000010.10 - 80080866	Oct 12, 2018 (152)
127	The Danish reference pan genome	NC_000010.10 - 80080866	Apr 26, 2020 (154)
128	gnomAD - Genomes	NC_000010.11 - 78321109	Apr 26, 2021 (155)
129	Genome of the Netherlands Release 5	NC_000010.10 - 80080866	Apr 26, 2020 (154)
130	HGDP-CEPH-db Supplement 1	NC_000010.9 - 79750872	Apr 26, 2020 (154)
131	HapMap	NC_000010.11 - 78321109	Apr 26, 2020 (154)
132	KOREAN population from KRGDB	NC_000010.10 - 80080866	Apr 26, 2020 (154)
133	Northern Sweden	NC_000010.10 - 80080866	Jul 13, 2019 (153)
134	The PAGE Study	NC_000010.11 - 78321109	Jul 13, 2019 (153)
135	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 80080866	Apr 26, 2021 (155)
136	Qatari	NC_000010.10 - 80080866	Apr 26, 2020 (154)
137	SGDP_PRJ	NC_000010.10 - 80080866	Apr 26, 2020 (154)
138	Siberian	NC_000010.10 - 80080866	Apr 26, 2020 (154)
139	8.3KJPN	NC_000010.10 - 80080866	Apr 26, 2021 (155)
140	14KJPN	NC_000010.11 - 78321109	Oct 16, 2022 (156)
141	TopMed	NC_000010.11 - 78321109	Apr 26, 2021 (155)
142	A Vietnamese Genetic Variation Database	NC_000010.10 - 80080866	Jul 13, 2019 (153)
143	ALFA	NC_000010.11 - 78321109	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)
rs58782888	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss85548251, ss85698462, ss3638946157, ss3639472908	NC_000010.8:79750871:C:T	NC_000010.11:78321108:C:T	(self)
57612, 69940, ss168609852, ss201745112, ss206996840, ss210767081, ss280688343, ss290875573, ss481718752, ss825605391, ss1397586150, ss1597353487, ss1713193548, ss2635016368, ss3642863071, ss3847392048	NC_000010.9:79750871:C:T	NC_000010.11:78321108:C:T	(self)
50577070, 55082, 19929199, 2233016, 12517229, 29864157, 10766268, 711910, 13087169, 26599391, 7040908, 56416624, 6233979, ss224823023, ss235246718, ss241940107, ss481750172, ss482716306, ss485654116, ss537531230, ss562071230, ss657014788, ss778990831, ss783272616, ss784225795, ss832533668, ss833142037, ss834453083, ss987678881, ss1077127062, ss1338162400, ss1426375932, ss1575223883, ss1751981897, ss1806470840, ss1931045239, ss1959276030, ss1967171390, ss2026249197, ss2154524554, ss2627593664, ss2632733703, ss2698771939, ss2710714274, ss2890817083, ss3006773191, ss3021255350, ss3349205303, ss3626485259, ss3630758047, ss3632955817, ss3633653281, ss3634412113, ss3635345650, ss3636095504, ss3637096342, ss3637860333, ss3640119455, ss3641003319, ss3641297615, ss3651611765, ss3674190951, ss3737481403, ss3744713099, ss3748323633, ss3772213492, ss3832217233, ss3839646511, ss3874582411, ss3922686763, ss3985485983, ss4017495160, ss5198447317, ss5237479821, ss5315486035, ss5394599824, ss5624252604, ss5649651828, ss5799817796, ss5824647055, ss5847376023, ss5847601834, ss5940932245, ss5979331584	NC_000010.10:80080865:C:T	NC_000010.11:78321108:C:T	(self)
66477635, 357417438, 442568, 790418, 78353673, 74183123, 2672662678, ss2176237736, ss3026914652, ss3690235827, ss3725171013, ss3771568949, ss3813693144, ss3845119569, ss4858637468, ss5284685414, ss5480196717, ss5578951700, ss5744516569, ss5811689128, ss5849645463, ss5879631426	NC_000010.11:78321108:C:T	NC_000010.11:78321108:C:T	(self)
ss12110923	NT_008583.15:28632037:C:T	NC_000010.11:78321108:C:T	(self)
ss66788784, ss67848082, ss68001968, ss70958581, ss71566531, ss75766250, ss76621099, ss79274873, ss84751121, ss102893834, ss122863378, ss154456512, ss159631150, ss160929195, ss172369169, ss174619337	NT_030059.13:30885329:C:T	NC_000010.11:78321108: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 rs7920472

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

rs7920472