Name: rs10749330
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.

rs10749330

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:119951720 (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=0.292512 (77425/264690, TOPMED)
T=0.334754 (59538/177856, ALFA)
T=0.300107 (42027/140040, GnomAD) (+ 19 more)
T=0.16144 (4562/28258, 14KJPN)
T=0.16366 (2743/16760, 8.3KJPN)
T=0.2512 (1609/6404, 1000G_30x)
T=0.2518 (1261/5008, 1000G)
T=0.3565 (1597/4480, Estonian)
T=0.3588 (1383/3854, ALSPAC)
T=0.3528 (1308/3708, TWINSUK)
T=0.1829 (536/2930, KOREAN)
T=0.2740 (571/2084, HGDP_Stanford)
T=0.2497 (472/1890, HapMap)
T=0.1779 (326/1832, Korea1K)
T=0.374 (373/998, GoNL)
T=0.320 (192/600, NorthernSweden)
T=0.195 (102/524, SGDP_PRJ)
T=0.370 (80/216, Qatari)
T=0.196 (42/214, Vietnamese)
T=0.41 (22/54, Ancient Sardinia)
T=0.42 (17/40, GENOME_DK)
T=0.28 (11/40, 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	177856	T=0.334754	C=0.665246
European	Sub	150730	T=0.347575	C=0.652425
African	Sub	7064	T=0.2075	C=0.7925
African Others	Sub	264	T=0.174	C=0.826
African American	Sub	6800	T=0.2088	C=0.7912
Asian	Sub	700	T=0.176	C=0.824
East Asian	Sub	554	T=0.186	C=0.814
Other Asian	Sub	146	T=0.137	C=0.863
Latin American 1	Sub	840	T=0.320	C=0.680
Latin American 2	Sub	6886	T=0.2668	C=0.7332
South Asian	Sub	5042	T=0.2721	C=0.7279
Other	Sub	6594	T=0.3156	C=0.6844

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=0.292512	C=0.707488
Allele Frequency Aggregator	Total	Global	177856	T=0.334754	C=0.665246
Allele Frequency Aggregator	European	Sub	150730	T=0.347575	C=0.652425
Allele Frequency Aggregator	African	Sub	7064	T=0.2075	C=0.7925
Allele Frequency Aggregator	Latin American 2	Sub	6886	T=0.2668	C=0.7332
Allele Frequency Aggregator	Other	Sub	6594	T=0.3156	C=0.6844
Allele Frequency Aggregator	South Asian	Sub	5042	T=0.2721	C=0.7279
Allele Frequency Aggregator	Latin American 1	Sub	840	T=0.320	C=0.680
Allele Frequency Aggregator	Asian	Sub	700	T=0.176	C=0.824
gnomAD - Genomes	Global	Study-wide	140040	T=0.300107	C=0.699893
gnomAD - Genomes	European	Sub	75836	T=0.35238	C=0.64762
gnomAD - Genomes	African	Sub	41984	T=0.21456	C=0.78544
gnomAD - Genomes	American	Sub	13620	T=0.29207	C=0.70793
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.3292	C=0.6708
gnomAD - Genomes	East Asian	Sub	3130	T=0.1850	C=0.8150
gnomAD - Genomes	Other	Sub	2150	T=0.3005	C=0.6995
14KJPN	JAPANESE	Study-wide	28258	T=0.16144	C=0.83856
8.3KJPN	JAPANESE	Study-wide	16760	T=0.16366	C=0.83634
1000Genomes_30x	Global	Study-wide	6404	T=0.2512	C=0.7488
1000Genomes_30x	African	Sub	1786	T=0.1982	C=0.8018
1000Genomes_30x	Europe	Sub	1266	T=0.3412	C=0.6588
1000Genomes_30x	South Asian	Sub	1202	T=0.2912	C=0.7088
1000Genomes_30x	East Asian	Sub	1170	T=0.1658	C=0.8342
1000Genomes_30x	American	Sub	980	T=0.285	C=0.715
1000Genomes	Global	Study-wide	5008	T=0.2518	C=0.7482
1000Genomes	African	Sub	1322	T=0.2035	C=0.7965
1000Genomes	East Asian	Sub	1008	T=0.1647	C=0.8353
1000Genomes	Europe	Sub	1006	T=0.3439	C=0.6561
1000Genomes	South Asian	Sub	978	T=0.291	C=0.709
1000Genomes	American	Sub	694	T=0.281	C=0.719
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.3565	C=0.6435
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.3588	C=0.6412
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3528	C=0.6472
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1829	A=0.0000, C=0.8171, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.2740	C=0.7260
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.217	C=0.783
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.302	C=0.698
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.351	C=0.649
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.338	C=0.662
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.223	C=0.777
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.167	C=0.833
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.32	C=0.68
HapMap	Global	Study-wide	1890	T=0.2497	C=0.7503
HapMap	American	Sub	770	T=0.278	C=0.722
HapMap	African	Sub	690	T=0.216	C=0.784
HapMap	Asian	Sub	254	T=0.169	C=0.831
HapMap	Europe	Sub	176	T=0.375	C=0.625
Korean Genome Project	KOREAN	Study-wide	1832	T=0.1779	C=0.8221
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.374	C=0.626
Northern Sweden	ACPOP	Study-wide	600	T=0.320	C=0.680
SGDP_PRJ	Global	Study-wide	524	T=0.195	C=0.805
Qatari	Global	Study-wide	216	T=0.370	C=0.630
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.196	C=0.804
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	54	T=0.41	C=0.59
The Danish reference pan genome	Danish	Study-wide	40	T=0.42	C=0.57
Siberian	Global	Study-wide	40	T=0.28	C=0.72

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.119951720T>A
GRCh38.p14 chr 10	NC_000010.11:g.119951720T>C
GRCh38.p14 chr 10	NC_000010.11:g.119951720T>G
GRCh37.p13 chr 10	NC_000010.10:g.121711232T>A
GRCh37.p13 chr 10	NC_000010.10:g.121711232T>C
GRCh37.p13 chr 10	NC_000010.10:g.121711232T>G

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 10	NC_000010.11:g.119951720=	NC_000010.11:g.119951720T>A	NC_000010.11:g.119951720T>C	NC_000010.11:g.119951720T>G
GRCh37.p13 chr 10	NC_000010.10:g.121711232=	NC_000010.10:g.121711232T>A	NC_000010.10:g.121711232T>C	NC_000010.10:g.121711232T>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#.

128 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss15478777	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss17400275	Feb 27, 2004 (120)
3	SC_SNP	ss18436986	Feb 27, 2004 (120)
4	SC_SNP	ss18651852	Feb 27, 2004 (120)
5	SC_SNP	ss18892136	Feb 27, 2004 (120)
6	SSAHASNP	ss20691129	Apr 05, 2004 (121)
7	ABI	ss38579550	Mar 13, 2006 (126)
8	ILLUMINA	ss66698714	Dec 01, 2006 (127)
9	ILLUMINA	ss66898054	Dec 01, 2006 (127)
10	ILLUMINA	ss67010150	Dec 01, 2006 (127)
11	ILLUMINA	ss70377900	May 18, 2007 (127)
12	ILLUMINA	ss70494132	May 24, 2008 (130)
13	ILLUMINA	ss71019059	May 18, 2007 (127)
14	ILLUMINA	ss75668795	Dec 07, 2007 (129)
15	KRIBB_YJKIM	ss84987401	Dec 14, 2007 (130)
16	HGSV	ss85388135	Dec 14, 2007 (130)
17	BCMHGSC_JDW	ss88378623	Mar 23, 2008 (129)
18	HUMANGENOME_JCVI	ss97689655	Feb 04, 2009 (130)
19	BGI	ss106706502	Feb 04, 2009 (130)
20	1000GENOMES	ss113906445	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss119314261	Feb 15, 2009 (130)
22	ILLUMINA	ss121378024	Dec 01, 2009 (131)
23	ENSEMBL	ss131847709	Dec 01, 2009 (131)
24	ENSEMBL	ss132130159	Dec 01, 2009 (131)
25	ILLUMINA	ss152805246	Dec 01, 2009 (131)
26	GMI	ss155619860	Dec 01, 2009 (131)
27	ILLUMINA	ss159139032	Dec 01, 2009 (131)
28	ILLUMINA	ss159914785	Dec 01, 2009 (131)
29	COMPLETE_GENOMICS	ss168772654	Jul 04, 2010 (132)
30	ILLUMINA	ss169588507	Jul 04, 2010 (132)
31	ILLUMINA	ss170447441	Jul 04, 2010 (132)
32	COMPLETE_GENOMICS	ss171212135	Jul 04, 2010 (132)
33	COMPLETE_GENOMICS	ss174778940	Jul 04, 2010 (132)
34	BUSHMAN	ss202096725	Jul 04, 2010 (132)
35	BCM-HGSC-SUB	ss207135594	Jul 04, 2010 (132)
36	1000GENOMES	ss210774872	Jul 14, 2010 (132)
37	1000GENOMES	ss224975970	Jul 14, 2010 (132)
38	1000GENOMES	ss235358315	Jul 15, 2010 (132)
39	1000GENOMES	ss242029360	Jul 15, 2010 (132)
40	GMI	ss280797200	May 04, 2012 (137)
41	GMI	ss286274178	Apr 25, 2013 (138)
42	PJP	ss290945152	May 09, 2011 (134)
43	ILLUMINA	ss479330691	May 04, 2012 (137)
44	ILLUMINA	ss479333777	May 04, 2012 (137)
45	ILLUMINA	ss479725005	Sep 08, 2015 (146)
46	ILLUMINA	ss484465561	May 04, 2012 (137)
47	ILLUMINA	ss536628301	Sep 08, 2015 (146)
48	TISHKOFF	ss562251370	Apr 25, 2013 (138)
49	SSMP	ss657467531	Apr 25, 2013 (138)
50	ILLUMINA	ss778362812	Aug 21, 2014 (142)
51	ILLUMINA	ss782679347	Aug 21, 2014 (142)
52	ILLUMINA	ss783647881	Aug 21, 2014 (142)
53	ILLUMINA	ss825347511	Apr 01, 2015 (144)
54	ILLUMINA	ss831930113	Apr 01, 2015 (144)
55	ILLUMINA	ss832651683	Aug 21, 2014 (142)
56	ILLUMINA	ss833242372	Aug 21, 2014 (142)
57	ILLUMINA	ss833817606	Aug 21, 2014 (142)
58	EVA-GONL	ss987990622	Aug 21, 2014 (142)
59	JMKIDD_LAB	ss1077347827	Aug 21, 2014 (142)
60	1000GENOMES	ss1339330097	Aug 21, 2014 (142)
61	DDI	ss1426462804	Apr 01, 2015 (144)
62	EVA_GENOME_DK	ss1575394032	Apr 01, 2015 (144)
63	EVA_DECODE	ss1597669732	Apr 01, 2015 (144)
64	EVA_UK10K_ALSPAC	ss1625579201	Apr 01, 2015 (144)
65	EVA_UK10K_TWINSUK	ss1668573234	Apr 01, 2015 (144)
66	EVA_SVP	ss1713216488	Apr 01, 2015 (144)
67	ILLUMINA	ss1751950681	Sep 08, 2015 (146)
68	HAMMER_LAB	ss1806597771	Sep 08, 2015 (146)
69	WEILL_CORNELL_DGM	ss1931347888	Feb 12, 2016 (147)
70	GENOMED	ss1967239207	Jul 19, 2016 (147)
71	JJLAB	ss2026410197	Sep 14, 2016 (149)
72	USC_VALOUEV	ss2154687127	Dec 20, 2016 (150)
73	HUMAN_LONGEVITY	ss2178630095	Dec 20, 2016 (150)
74	SYSTEMSBIOZJU	ss2627671711	Nov 08, 2017 (151)
75	ILLUMINA	ss2632770569	Nov 08, 2017 (151)
76	ILLUMINA	ss2635019693	Nov 08, 2017 (151)
77	GRF	ss2698947564	Nov 08, 2017 (151)
78	GNOMAD	ss2894143214	Nov 08, 2017 (151)
79	SWEGEN	ss3007254484	Nov 08, 2017 (151)
80	BIOINF_KMB_FNS_UNIBA	ss3026993719	Nov 08, 2017 (151)
81	CSHL	ss3349340703	Nov 08, 2017 (151)
82	ILLUMINA	ss3626549400	Oct 12, 2018 (152)
83	ILLUMINA	ss3630792326	Oct 12, 2018 (152)
84	ILLUMINA	ss3632967093	Oct 12, 2018 (152)
85	ILLUMINA	ss3633665014	Oct 12, 2018 (152)
86	ILLUMINA	ss3634427321	Oct 12, 2018 (152)
87	ILLUMINA	ss3635357123	Oct 12, 2018 (152)
88	ILLUMINA	ss3636111943	Oct 12, 2018 (152)
89	ILLUMINA	ss3637107871	Oct 12, 2018 (152)
90	ILLUMINA	ss3637877954	Oct 12, 2018 (152)
91	ILLUMINA	ss3638954197	Oct 12, 2018 (152)
92	ILLUMINA	ss3639477379	Oct 12, 2018 (152)
93	ILLUMINA	ss3640134662	Oct 12, 2018 (152)
94	ILLUMINA	ss3642878876	Oct 12, 2018 (152)
95	URBANLAB	ss3649480915	Oct 12, 2018 (152)
96	EGCUT_WGS	ss3674673262	Jul 13, 2019 (153)
97	EVA_DECODE	ss3690812469	Jul 13, 2019 (153)
98	ACPOP	ss3737735904	Jul 13, 2019 (153)
99	ILLUMINA	ss3744728294	Jul 13, 2019 (153)
100	EVA	ss3748686062	Jul 13, 2019 (153)
101	ILLUMINA	ss3772228524	Jul 13, 2019 (153)
102	PACBIO	ss3786805324	Jul 13, 2019 (153)
103	PACBIO	ss3791964790	Jul 13, 2019 (153)
104	PACBIO	ss3796846934	Jul 13, 2019 (153)
105	KHV_HUMAN_GENOMES	ss3814042928	Jul 13, 2019 (153)
106	EVA	ss3832365530	Apr 26, 2020 (154)
107	EVA	ss3839723773	Apr 26, 2020 (154)
108	EVA	ss3845198456	Apr 26, 2020 (154)
109	HGDP	ss3847401797	Apr 26, 2020 (154)
110	SGDP_PRJ	ss3875193286	Apr 26, 2020 (154)
111	KRGDB	ss3923372056	Apr 26, 2020 (154)
112	KOGIC	ss3968806038	Apr 26, 2020 (154)
113	EVA	ss3985504456	Apr 26, 2021 (155)
114	EVA	ss4017511471	Apr 26, 2021 (155)
115	TOPMED	ss4868809202	Apr 26, 2021 (155)
116	TOMMO_GENOMICS	ss5199774999	Apr 26, 2021 (155)
117	1000G_HIGH_COVERAGE	ss5285700612	Oct 16, 2022 (156)
118	EVA	ss5315507491	Oct 16, 2022 (156)
119	HUGCELL_USP	ss5481100029	Oct 16, 2022 (156)
120	1000G_HIGH_COVERAGE	ss5580497368	Oct 16, 2022 (156)
121	SANFORD_IMAGENETICS	ss5650228979	Oct 16, 2022 (156)
122	TOMMO_GENOMICS	ss5746233322	Oct 16, 2022 (156)
123	EVA	ss5799826998	Oct 16, 2022 (156)
124	YY_MCH	ss5811940856	Oct 16, 2022 (156)
125	EVA	ss5825049051	Oct 16, 2022 (156)
126	EVA	ss5849768977	Oct 16, 2022 (156)
127	EVA	ss5880799653	Oct 16, 2022 (156)
128	EVA	ss5941535406	Oct 16, 2022 (156)
129	1000Genomes	NC_000010.10 - 121711232	Oct 12, 2018 (152)
130	1000Genomes_30x	NC_000010.11 - 119951720	Oct 16, 2022 (156)
131	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 121711232	Oct 12, 2018 (152)
132	Genetic variation in the Estonian population	NC_000010.10 - 121711232	Oct 12, 2018 (152)
133	The Danish reference pan genome	NC_000010.10 - 121711232	Apr 26, 2020 (154)
134	gnomAD - Genomes	NC_000010.11 - 119951720	Apr 26, 2021 (155)
135	Genome of the Netherlands Release 5	NC_000010.10 - 121711232	Apr 26, 2020 (154)
136	HGDP-CEPH-db Supplement 1	NC_000010.9 - 121701222	Apr 26, 2020 (154)
137	HapMap	NC_000010.11 - 119951720	Apr 26, 2020 (154)
138	KOREAN population from KRGDB	NC_000010.10 - 121711232	Apr 26, 2020 (154)
139	Korean Genome Project	NC_000010.11 - 119951720	Apr 26, 2020 (154)
140	Northern Sweden	NC_000010.10 - 121711232	Jul 13, 2019 (153)
141	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 121711232	Apr 26, 2021 (155)
142	Qatari	NC_000010.10 - 121711232	Apr 26, 2020 (154)
143	SGDP_PRJ	NC_000010.10 - 121711232	Apr 26, 2020 (154)
144	Siberian	NC_000010.10 - 121711232	Apr 26, 2020 (154)
145	8.3KJPN	NC_000010.10 - 121711232	Apr 26, 2021 (155)
146	14KJPN	NC_000010.11 - 119951720	Oct 16, 2022 (156)
147	TopMed	NC_000010.11 - 119951720	Apr 26, 2021 (155)
148	UK 10K study - Twins	NC_000010.10 - 121711232	Oct 12, 2018 (152)
149	A Vietnamese Genetic Variation Database	NC_000010.10 - 121711232	Jul 13, 2019 (153)
150	ALFA	NC_000010.11 - 119951720	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)
rs57973410	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
30549450, ss3923372056	NC_000010.10:121711231:T:A	NC_000010.11:119951719:T:A	(self)
ss85388135, ss3638954197, ss3639477379	NC_000010.8:121701221:T:C	NC_000010.11:119951719:T:C	(self)
79689, ss88378623, ss113906445, ss119314261, ss159914785, ss168772654, ss171212135, ss174778940, ss202096725, ss207135594, ss210774872, ss280797200, ss286274178, ss290945152, ss479330691, ss825347511, ss1597669732, ss1713216488, ss2635019693, ss3642878876, ss3847401797	NC_000010.9:121701221:T:C	NC_000010.11:119951719:T:C	(self)
51786810, 28767178, 20411510, 2353132, 12820602, 30549450, 11020769, 730383, 13389818, 27210266, 7203481, 57744306, 28767178, 6382449, ss224975970, ss235358315, ss242029360, ss479333777, ss479725005, ss484465561, ss536628301, ss562251370, ss657467531, ss778362812, ss782679347, ss783647881, ss831930113, ss832651683, ss833242372, ss833817606, ss987990622, ss1077347827, ss1339330097, ss1426462804, ss1575394032, ss1625579201, ss1668573234, ss1751950681, ss1806597771, ss1931347888, ss1967239207, ss2026410197, ss2154687127, ss2627671711, ss2632770569, ss2698947564, ss2894143214, ss3007254484, ss3349340703, ss3626549400, ss3630792326, ss3632967093, ss3633665014, ss3634427321, ss3635357123, ss3636111943, ss3637107871, ss3637877954, ss3640134662, ss3674673262, ss3737735904, ss3744728294, ss3748686062, ss3772228524, ss3786805324, ss3791964790, ss3796846934, ss3832365530, ss3839723773, ss3875193286, ss3923372056, ss3985504456, ss4017511471, ss5199774999, ss5315507491, ss5650228979, ss5799826998, ss5825049051, ss5941535406	NC_000010.10:121711231:T:C	NC_000010.11:119951719:T:C	(self)
68023303, 365902971, 506991, 25184039, 80070426, 84354857, 9054410161, ss2178630095, ss3026993719, ss3649480915, ss3690812469, ss3814042928, ss3845198456, ss3968806038, ss4868809202, ss5285700612, ss5481100029, ss5580497368, ss5746233322, ss5811940856, ss5849768977, ss5880799653	NC_000010.11:119951719:T:C	NC_000010.11:119951719:T:C	(self)
ss15478777, ss17400275, ss18436986, ss18651852, ss18892136, ss20691129	NT_030059.11:40459757:T:C	NC_000010.11:119951719:T:C	(self)
ss38579550, ss66698714, ss66898054, ss67010150, ss70377900, ss70494132, ss71019059, ss75668795, ss84987401, ss97689655, ss106706502, ss121378024, ss131847709, ss132130159, ss152805246, ss155619860, ss159139032, ss169588507, ss170447441	NT_030059.13:72515695:T:C	NC_000010.11:119951719:T:C	(self)
30549450, ss3923372056	NC_000010.10:121711231:T:G	NC_000010.11:119951719: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 rs10749330

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

rs10749330