Name: rs1370270
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.

rs1370270

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:55882927 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.123684 (32738/264690, TOPMED)
A=0.180011 (36004/200010, ALFA)
A=0.134566 (18860/140154, GnomAD) (+ 20 more)
A=0.00000 (0/28258, 14KJPN)
A=0.00006 (1/16760, 8.3KJPN)
A=0.0664 (425/6404, 1000G_30x)
A=0.0669 (335/5008, 1000G)
A=0.1779 (797/4480, Estonian)
A=0.2081 (802/3854, ALSPAC)
A=0.2069 (767/3708, TWINSUK)
A=0.0007 (2/2930, KOREAN)
A=0.0369 (77/2084, HGDP_Stanford)
A=0.0000 (0/1832, Korea1K)
A=0.0723 (82/1134, Daghestan)
A=0.222 (222/998, GoNL)
A=0.091 (90/984, HapMap)
A=0.173 (104/600, NorthernSweden)
A=0.036 (20/554, SGDP_PRJ)
A=0.037 (8/216, Qatari)
A=0.000 (0/216, Vietnamese)
A=0.07 (4/56, Siberian)
A=0.25 (12/48, Ancient Sardinia)
A=0.20 (8/40, 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	200010	A=0.180011	G=0.819989
European	Sub	172756	A=0.195843	G=0.804157
African	Sub	7096	A=0.0351	G=0.9649
African Others	Sub	264	A=0.004	G=0.996
African American	Sub	6832	A=0.0363	G=0.9637
Asian	Sub	704	A=0.004	G=0.996
East Asian	Sub	558	A=0.000	G=1.000
Other Asian	Sub	146	A=0.021	G=0.979
Latin American 1	Sub	844	A=0.122	G=0.878
Latin American 2	Sub	6908	A=0.1019	G=0.8981
South Asian	Sub	5044	A=0.0303	G=0.9697
Other	Sub	6658	A=0.1440	G=0.8560

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=0.123684	G=0.876316
Allele Frequency Aggregator	Total	Global	200010	A=0.180011	G=0.819989
Allele Frequency Aggregator	European	Sub	172756	A=0.195843	G=0.804157
Allele Frequency Aggregator	African	Sub	7096	A=0.0351	G=0.9649
Allele Frequency Aggregator	Latin American 2	Sub	6908	A=0.1019	G=0.8981
Allele Frequency Aggregator	Other	Sub	6658	A=0.1440	G=0.8560
Allele Frequency Aggregator	South Asian	Sub	5044	A=0.0303	G=0.9697
Allele Frequency Aggregator	Latin American 1	Sub	844	A=0.122	G=0.878
Allele Frequency Aggregator	Asian	Sub	704	A=0.004	G=0.996
gnomAD - Genomes	Global	Study-wide	140154	A=0.134566	G=0.865434
gnomAD - Genomes	European	Sub	75884	A=0.19792	G=0.80208
gnomAD - Genomes	African	Sub	42024	A=0.03586	G=0.96414
gnomAD - Genomes	American	Sub	13640	A=0.12691	G=0.87309
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.0966	G=0.9034
gnomAD - Genomes	East Asian	Sub	3128	A=0.0010	G=0.9990
gnomAD - Genomes	Other	Sub	2154	A=0.1295	G=0.8705
14KJPN	JAPANESE	Study-wide	28258	A=0.00000	G=1.00000
8.3KJPN	JAPANESE	Study-wide	16760	A=0.00006	G=0.99994
1000Genomes_30x	Global	Study-wide	6404	A=0.0664	G=0.9336
1000Genomes_30x	African	Sub	1786	A=0.0056	G=0.9944
1000Genomes_30x	Europe	Sub	1266	A=0.2204	G=0.7796
1000Genomes_30x	South Asian	Sub	1202	A=0.0300	G=0.9700
1000Genomes_30x	East Asian	Sub	1170	A=0.0000	G=1.0000
1000Genomes_30x	American	Sub	980	A=0.102	G=0.898
1000Genomes	Global	Study-wide	5008	A=0.0669	G=0.9331
1000Genomes	African	Sub	1322	A=0.0068	G=0.9932
1000Genomes	East Asian	Sub	1008	A=0.0000	G=1.0000
1000Genomes	Europe	Sub	1006	A=0.2266	G=0.7734
1000Genomes	South Asian	Sub	978	A=0.028	G=0.972
1000Genomes	American	Sub	694	A=0.102	G=0.898
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.1779	G=0.8221
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.2081	G=0.7919
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.2069	G=0.7931
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.0007	G=0.9993
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.0369	G=0.9631
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.004	G=0.996
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.017	G=0.983
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.029	G=0.971
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.169	G=0.831
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.004	G=0.996
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.014	G=0.986
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.00	G=1.00
Korean Genome Project	KOREAN	Study-wide	1832	A=0.0000	G=1.0000
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	A=0.0723	G=0.9277
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	A=0.062	G=0.938
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.069	G=0.931
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.090	G=0.910
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.176	G=0.824
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.01	G=0.99
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.06	G=0.94
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.222	G=0.778
HapMap	Global	Study-wide	984	A=0.091	G=0.909
HapMap	American	Sub	600	A=0.110	G=0.890
HapMap	Europe	Sub	176	A=0.136	G=0.864
HapMap	African	Sub	120	A=0.000	G=1.000
HapMap	Asian	Sub	88	A=0.00	G=1.00
Northern Sweden	ACPOP	Study-wide	600	A=0.173	G=0.827
SGDP_PRJ	Global	Study-wide	554	A=0.036	G=0.964
Qatari	Global	Study-wide	216	A=0.037	G=0.963
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.000	G=1.000
Siberian	Global	Study-wide	56	A=0.07	G=0.93
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	48	A=0.25	G=0.75
The Danish reference pan genome	Danish	Study-wide	40	A=0.20	G=0.80

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 20	NC_000020.11:g.55882927A>G
GRCh37.p13 chr 20	NC_000020.10:g.54457983A>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	A=	G
GRCh38.p14 chr 20	NC_000020.11:g.55882927=	NC_000020.11:g.55882927A>G
GRCh37.p13 chr 20	NC_000020.10:g.54457983=	NC_000020.10:g.54457983A>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#.

131 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2156767	Oct 23, 2000 (88)
2	SC_SNP	ss8457459	Apr 21, 2003 (114)
3	BCM_SSAHASNP	ss10966646	Jul 11, 2003 (116)
4	CSHL-HAPMAP	ss16899532	Feb 27, 2004 (120)
5	SSAHASNP	ss21755283	Apr 05, 2004 (121)
6	PERLEGEN	ss24439132	Sep 20, 2004 (123)
7	ABI	ss44237963	Mar 15, 2006 (126)
8	ILLUMINA	ss66575533	Dec 01, 2006 (127)
9	ILLUMINA	ss67088249	Dec 01, 2006 (127)
10	ILLUMINA	ss67421852	Dec 01, 2006 (127)
11	PERLEGEN	ss69245319	May 18, 2007 (127)
12	ILLUMINA	ss70426910	May 18, 2007 (127)
13	ILLUMINA	ss70609873	May 26, 2008 (130)
14	ILLUMINA	ss71157152	May 18, 2007 (127)
15	ILLUMINA	ss74923112	Dec 05, 2007 (129)
16	KRIBB_YJKIM	ss83741712	Dec 15, 2007 (130)
17	HGSV	ss84842405	Dec 15, 2007 (130)
18	BCMHGSC_JDW	ss91734195	Mar 24, 2008 (129)
19	BGI	ss106195107	Feb 06, 2009 (130)
20	1000GENOMES	ss112144718	Jan 25, 2009 (130)
21	1000GENOMES	ss113484322	Jan 25, 2009 (130)
22	ILLUMINA-UK	ss117586467	Feb 14, 2009 (130)
23	ILLUMINA	ss121664245	Dec 01, 2009 (131)
24	ENSEMBL	ss135687824	Dec 01, 2009 (131)
25	ENSEMBL	ss138261705	Dec 01, 2009 (131)
26	ILLUMINA	ss153395523	Dec 01, 2009 (131)
27	GMI	ss156547729	Dec 01, 2009 (131)
28	ILLUMINA	ss159261445	Dec 01, 2009 (131)
29	ILLUMINA	ss160343089	Dec 01, 2009 (131)
30	COMPLETE_GENOMICS	ss168313982	Jul 04, 2010 (132)
31	COMPLETE_GENOMICS	ss169924330	Jul 04, 2010 (132)
32	ILLUMINA	ss170423585	Jul 04, 2010 (132)
33	COMPLETE_GENOMICS	ss172166014	Jul 04, 2010 (132)
34	ILLUMINA	ss172449285	Jul 04, 2010 (132)
35	BUSHMAN	ss203925113	Jul 04, 2010 (132)
36	BCM-HGSC-SUB	ss208589111	Jul 04, 2010 (132)
37	1000GENOMES	ss228415043	Jul 14, 2010 (132)
38	1000GENOMES	ss237874880	Jul 15, 2010 (132)
39	1000GENOMES	ss244037785	Jul 15, 2010 (132)
40	BL	ss255726243	May 09, 2011 (134)
41	GMI	ss283424257	May 04, 2012 (137)
42	GMI	ss287475741	Apr 25, 2013 (138)
43	PJP	ss292585331	May 09, 2011 (134)
44	ILLUMINA	ss479944162	May 04, 2012 (137)
45	ILLUMINA	ss479952485	May 04, 2012 (137)
46	ILLUMINA	ss480590502	Sep 08, 2015 (146)
47	ILLUMINA	ss484770330	May 04, 2012 (137)
48	ILLUMINA	ss536859863	Sep 08, 2015 (146)
49	TISHKOFF	ss566326456	Apr 25, 2013 (138)
50	SSMP	ss662205621	Apr 25, 2013 (138)
51	ILLUMINA	ss778803463	Sep 08, 2015 (146)
52	ILLUMINA	ss782831873	Sep 08, 2015 (146)
53	ILLUMINA	ss783796670	Sep 08, 2015 (146)
54	ILLUMINA	ss825396184	Apr 01, 2015 (144)
55	ILLUMINA	ss832085384	Sep 08, 2015 (146)
56	ILLUMINA	ss832773666	Jul 13, 2019 (153)
57	ILLUMINA	ss834263656	Sep 08, 2015 (146)
58	EVA-GONL	ss994842341	Aug 21, 2014 (142)
59	JMKIDD_LAB	ss1082292759	Aug 21, 2014 (142)
60	1000GENOMES	ss1365240519	Aug 21, 2014 (142)
61	HAMMER_LAB	ss1397772532	Sep 08, 2015 (146)
62	DDI	ss1429087434	Apr 01, 2015 (144)
63	EVA_GENOME_DK	ss1579552221	Apr 01, 2015 (144)
64	EVA_UK10K_ALSPAC	ss1639031484	Apr 01, 2015 (144)
65	EVA_UK10K_TWINSUK	ss1682025517	Apr 01, 2015 (144)
66	EVA_DECODE	ss1698905954	Apr 01, 2015 (144)
67	EVA_SVP	ss1713703273	Apr 01, 2015 (144)
68	ILLUMINA	ss1752393143	Sep 08, 2015 (146)
69	HAMMER_LAB	ss1809555922	Sep 08, 2015 (146)
70	WEILL_CORNELL_DGM	ss1938361188	Feb 12, 2016 (147)
71	GENOMED	ss1969158293	Jul 19, 2016 (147)
72	JJLAB	ss2029960127	Sep 14, 2016 (149)
73	ILLUMINA	ss2095116565	Dec 20, 2016 (150)
74	USC_VALOUEV	ss2158530513	Dec 20, 2016 (150)
75	HUMAN_LONGEVITY	ss2243721517	Dec 20, 2016 (150)
76	SYSTEMSBIOZJU	ss2629474320	Nov 08, 2017 (151)
77	ILLUMINA	ss2633814994	Nov 08, 2017 (151)
78	GRF	ss2704227193	Nov 08, 2017 (151)
79	GNOMAD	ss2968748160	Nov 08, 2017 (151)
80	SWEGEN	ss3018374445	Nov 08, 2017 (151)
81	BIOINF_KMB_FNS_UNIBA	ss3028813338	Nov 08, 2017 (151)
82	CSHL	ss3352565097	Nov 08, 2017 (151)
83	ILLUMINA	ss3628420639	Oct 12, 2018 (152)
84	ILLUMINA	ss3631770549	Oct 12, 2018 (152)
85	ILLUMINA	ss3633255551	Oct 12, 2018 (152)
86	ILLUMINA	ss3633969922	Oct 12, 2018 (152)
87	ILLUMINA	ss3634842061	Oct 12, 2018 (152)
88	ILLUMINA	ss3635654907	Oct 12, 2018 (152)
89	ILLUMINA	ss3636536233	Oct 12, 2018 (152)
90	ILLUMINA	ss3637407018	Oct 12, 2018 (152)
91	ILLUMINA	ss3638353191	Oct 12, 2018 (152)
92	ILLUMINA	ss3639179940	Oct 12, 2018 (152)
93	ILLUMINA	ss3639604483	Oct 12, 2018 (152)
94	ILLUMINA	ss3640549359	Oct 12, 2018 (152)
95	ILLUMINA	ss3643315381	Oct 12, 2018 (152)
96	URBANLAB	ss3651043547	Oct 12, 2018 (152)
97	ILLUMINA	ss3652587949	Oct 12, 2018 (152)
98	EGCUT_WGS	ss3685058800	Jul 13, 2019 (153)
99	EVA_DECODE	ss3707185341	Jul 13, 2019 (153)
100	ACPOP	ss3743496138	Jul 13, 2019 (153)
101	ILLUMINA	ss3745141952	Jul 13, 2019 (153)
102	EVA	ss3758788433	Jul 13, 2019 (153)
103	ILLUMINA	ss3772638103	Jul 13, 2019 (153)
104	PACBIO	ss3788679497	Jul 13, 2019 (153)
105	PACBIO	ss3793565264	Jul 13, 2019 (153)
106	PACBIO	ss3798452587	Jul 13, 2019 (153)
107	KHV_HUMAN_GENOMES	ss3821947596	Jul 13, 2019 (153)
108	EVA	ss3835732362	Apr 27, 2020 (154)
109	EVA	ss3841490245	Apr 27, 2020 (154)
110	EVA	ss3847003664	Apr 27, 2020 (154)
111	HGDP	ss3847671531	Apr 27, 2020 (154)
112	SGDP_PRJ	ss3889349786	Apr 27, 2020 (154)
113	KRGDB	ss3939665053	Apr 27, 2020 (154)
114	KOGIC	ss3982521520	Apr 27, 2020 (154)
115	EVA	ss3985887284	Apr 26, 2021 (155)
116	EVA	ss4017854564	Apr 26, 2021 (155)
117	TOPMED	ss5092665201	Apr 26, 2021 (155)
118	TOMMO_GENOMICS	ss5230190118	Apr 26, 2021 (155)
119	1000G_HIGH_COVERAGE	ss5309218421	Oct 16, 2022 (156)
120	EVA	ss5316017348	Oct 16, 2022 (156)
121	EVA	ss5438164179	Oct 16, 2022 (156)
122	HUGCELL_USP	ss5501456854	Oct 16, 2022 (156)
123	1000G_HIGH_COVERAGE	ss5615874334	Oct 16, 2022 (156)
124	SANFORD_IMAGENETICS	ss5663446310	Oct 16, 2022 (156)
125	TOMMO_GENOMICS	ss5790160379	Oct 16, 2022 (156)
126	EVA	ss5800025692	Oct 16, 2022 (156)
127	YY_MCH	ss5818147364	Oct 16, 2022 (156)
128	EVA	ss5845855677	Oct 16, 2022 (156)
129	EVA	ss5853192265	Oct 16, 2022 (156)
130	EVA	ss5923905848	Oct 16, 2022 (156)
131	EVA	ss5958374188	Oct 16, 2022 (156)
132	1000Genomes	NC_000020.10 - 54457983	Oct 12, 2018 (152)
133	1000Genomes_30x	NC_000020.11 - 55882927	Oct 16, 2022 (156)
134	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 54457983	Oct 12, 2018 (152)
135	Genome-wide autozygosity in Daghestan	NC_000020.9 - 53891390	Apr 27, 2020 (154)
136	Genetic variation in the Estonian population	NC_000020.10 - 54457983	Oct 12, 2018 (152)
137	The Danish reference pan genome	NC_000020.10 - 54457983	Apr 27, 2020 (154)
138	gnomAD - Genomes	NC_000020.11 - 55882927	Apr 26, 2021 (155)
139	Genome of the Netherlands Release 5	NC_000020.10 - 54457983	Apr 27, 2020 (154)
140	HGDP-CEPH-db Supplement 1	NC_000020.9 - 53891390	Apr 27, 2020 (154)
141	HapMap	NC_000020.11 - 55882927	Apr 27, 2020 (154)
142	KOREAN population from KRGDB	NC_000020.10 - 54457983	Apr 27, 2020 (154)
143	Korean Genome Project	NC_000020.11 - 55882927	Apr 27, 2020 (154)
144	Northern Sweden	NC_000020.10 - 54457983	Jul 13, 2019 (153)
145	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000020.10 - 54457983	Apr 26, 2021 (155)
146	Qatari	NC_000020.10 - 54457983	Apr 27, 2020 (154)
147	SGDP_PRJ	NC_000020.10 - 54457983	Apr 27, 2020 (154)
148	Siberian	NC_000020.10 - 54457983	Apr 27, 2020 (154)
149	8.3KJPN	NC_000020.10 - 54457983	Apr 26, 2021 (155)
150	14KJPN	NC_000020.11 - 55882927	Oct 16, 2022 (156)
151	TopMed	NC_000020.11 - 55882927	Apr 26, 2021 (155)
152	UK 10K study - Twins	NC_000020.10 - 54457983	Oct 12, 2018 (152)
153	A Vietnamese Genetic Variation Database	NC_000020.10 - 54457983	Jul 13, 2019 (153)
154	ALFA	NC_000020.11 - 55882927	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)
rs17422475	Oct 07, 2004 (123)
rs60461429	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
286624, 349423, ss84842405, ss91734195, ss112144718, ss113484322, ss117586467, ss168313982, ss169924330, ss172166014, ss203925113, ss208589111, ss255726243, ss283424257, ss287475741, ss292585331, ss479944162, ss825396184, ss1397772532, ss1698905954, ss1713703273, ss3639179940, ss3639604483, ss3643315381, ss3847671531	NC_000020.9:53891389:A:G	NC_000020.11:55882926:A:G	(self)
78720442, 43584591, 30797048, 5717160, 19411530, 46842447, 16781003, 1113211, 20403110, 41366766, 11046867, 88159425, 43584591, 9612648, ss228415043, ss237874880, ss244037785, ss479952485, ss480590502, ss484770330, ss536859863, ss566326456, ss662205621, ss778803463, ss782831873, ss783796670, ss832085384, ss832773666, ss834263656, ss994842341, ss1082292759, ss1365240519, ss1429087434, ss1579552221, ss1639031484, ss1682025517, ss1752393143, ss1809555922, ss1938361188, ss1969158293, ss2029960127, ss2095116565, ss2158530513, ss2629474320, ss2633814994, ss2704227193, ss2968748160, ss3018374445, ss3352565097, ss3628420639, ss3631770549, ss3633255551, ss3633969922, ss3634842061, ss3635654907, ss3636536233, ss3637407018, ss3638353191, ss3640549359, ss3652587949, ss3685058800, ss3743496138, ss3745141952, ss3758788433, ss3772638103, ss3788679497, ss3793565264, ss3798452587, ss3835732362, ss3841490245, ss3889349786, ss3939665053, ss3985887284, ss4017854564, ss5230190118, ss5316017348, ss5438164179, ss5663446310, ss5800025692, ss5845855677, ss5958374188	NC_000020.10:54457982:A:G	NC_000020.11:55882926:A:G	(self)
103400269, 555251511, 2153181, 38899521, 123997483, 367774146, 3583174318, ss2243721517, ss3028813338, ss3651043547, ss3707185341, ss3821947596, ss3847003664, ss3982521520, ss5092665201, ss5309218421, ss5501456854, ss5615874334, ss5790160379, ss5818147364, ss5853192265, ss5923905848	NC_000020.11:55882926:A:G	NC_000020.11:55882926:A:G	(self)
ss10966646, ss16899532, ss21755283	NT_011362.8:19510890:A:G	NC_000020.11:55882926:A:G	(self)
ss2156767, ss8457459, ss24439132, ss44237963, ss66575533, ss67088249, ss67421852, ss69245319, ss70426910, ss70609873, ss71157152, ss74923112, ss83741712, ss106195107, ss121664245, ss135687824, ss138261705, ss153395523, ss156547729, ss159261445, ss160343089, ss170423585, ss172449285	NT_011362.10:24654074:A:G	NC_000020.11:55882926: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 rs1370270

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1370270