Name: rs1715364
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.

rs1715364

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:4918250 (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: T=0.443523 (117396/264690, TOPMED)
C=0.469754 (95236/202736, ALFA)
T=0.443302 (62064/140004, GnomAD) (+ 20 more)
T=0.31269 (8836/28258, 14KJPN)
T=0.31289 (5244/16760, 8.3KJPN)
T=0.3960 (2536/6404, 1000G_30x)
T=0.3990 (1998/5008, 1000G)
T=0.4446 (1992/4480, Estonian)
C=0.4414 (1701/3854, ALSPAC)
C=0.4420 (1639/3708, TWINSUK)
T=0.3256 (954/2930, KOREAN)
T=0.4227 (881/2084, HGDP_Stanford)
T=0.3488 (660/1892, HapMap)
T=0.3204 (587/1832, Korea1K)
C=0.457 (456/998, GoNL)
T=0.357 (283/792, PRJEB37584)
C=0.495 (297/600, NorthernSweden)
T=0.279 (124/444, SGDP_PRJ)
T=0.458 (99/216, Qatari)
T=0.429 (91/212, Vietnamese)
T=0.23 (11/48, Siberian)
C=0.45 (18/40, GENOME_DK)
C=0.33 (4/12, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC23A2 : Intron Variant
Publications: 2 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	202736	T=0.530246	C=0.469754
European	Sub	175472	T=0.543528	C=0.456472
African	Sub	7088	T=0.2506	C=0.7494
African Others	Sub	264	T=0.186	C=0.814
African American	Sub	6824	T=0.2531	C=0.7469
Asian	Sub	702	T=0.349	C=0.651
East Asian	Sub	556	T=0.360	C=0.640
Other Asian	Sub	146	T=0.308	C=0.692
Latin American 1	Sub	842	T=0.420	C=0.580
Latin American 2	Sub	6884	T=0.5436	C=0.4564
South Asian	Sub	5042	T=0.5194	C=0.4806
Other	Sub	6706	T=0.5055	C=0.4945

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=0.443523	C=0.556477
Allele Frequency Aggregator	Total	Global	202736	T=0.530246	C=0.469754
Allele Frequency Aggregator	European	Sub	175472	T=0.543528	C=0.456472
Allele Frequency Aggregator	African	Sub	7088	T=0.2506	C=0.7494
Allele Frequency Aggregator	Latin American 2	Sub	6884	T=0.5436	C=0.4564
Allele Frequency Aggregator	Other	Sub	6706	T=0.5055	C=0.4945
Allele Frequency Aggregator	South Asian	Sub	5042	T=0.5194	C=0.4806
Allele Frequency Aggregator	Latin American 1	Sub	842	T=0.420	C=0.580
Allele Frequency Aggregator	Asian	Sub	702	T=0.349	C=0.651
gnomAD - Genomes	Global	Study-wide	140004	T=0.443302	C=0.556698
gnomAD - Genomes	European	Sub	75836	T=0.53544	C=0.46456
gnomAD - Genomes	African	Sub	41946	T=0.25600	C=0.74400
gnomAD - Genomes	American	Sub	13618	T=0.51072	C=0.48928
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.5048	C=0.4952
gnomAD - Genomes	East Asian	Sub	3132	T=0.3605	C=0.6395
gnomAD - Genomes	Other	Sub	2148	T=0.4460	C=0.5540
14KJPN	JAPANESE	Study-wide	28258	T=0.31269	C=0.68731
8.3KJPN	JAPANESE	Study-wide	16760	T=0.31289	C=0.68711
1000Genomes_30x	Global	Study-wide	6404	T=0.3960	C=0.6040
1000Genomes_30x	African	Sub	1786	T=0.1769	C=0.8231
1000Genomes_30x	Europe	Sub	1266	T=0.5379	C=0.4621
1000Genomes_30x	South Asian	Sub	1202	T=0.5308	C=0.4692
1000Genomes_30x	East Asian	Sub	1170	T=0.3316	C=0.6684
1000Genomes_30x	American	Sub	980	T=0.523	C=0.477
1000Genomes	Global	Study-wide	5008	T=0.3990	C=0.6010
1000Genomes	African	Sub	1322	T=0.1846	C=0.8154
1000Genomes	East Asian	Sub	1008	T=0.3343	C=0.6657
1000Genomes	Europe	Sub	1006	T=0.5358	C=0.4642
1000Genomes	South Asian	Sub	978	T=0.529	C=0.471
1000Genomes	American	Sub	694	T=0.520	C=0.480
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4446	C=0.5554
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5586	C=0.4414
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5580	C=0.4420
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3256	A=0.0000, C=0.6744
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.4227	C=0.5773
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.353	C=0.647
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.505	C=0.495
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.469	C=0.531
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.547	C=0.453
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.136	C=0.864
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.444	C=0.556
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.53	C=0.47
HapMap	Global	Study-wide	1892	T=0.3488	C=0.6512
HapMap	American	Sub	770	T=0.447	C=0.553
HapMap	African	Sub	692	T=0.227	C=0.773
HapMap	Asian	Sub	254	T=0.283	C=0.717
HapMap	Europe	Sub	176	T=0.494	C=0.506
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3204	C=0.6796
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.543	C=0.457
CNV burdens in cranial meningiomas	Global	Study-wide	792	T=0.357	C=0.643
CNV burdens in cranial meningiomas	CRM	Sub	792	T=0.357	C=0.643
Northern Sweden	ACPOP	Study-wide	600	T=0.505	C=0.495
SGDP_PRJ	Global	Study-wide	444	T=0.279	C=0.721
Qatari	Global	Study-wide	216	T=0.458	C=0.542
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.429	C=0.571
Siberian	Global	Study-wide	48	T=0.23	C=0.77
The Danish reference pan genome	Danish	Study-wide	40	T=0.55	C=0.45
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	12	T=0.67	C=0.33

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.4918250T>A
GRCh38.p14 chr 20	NC_000020.11:g.4918250T>C
GRCh37.p13 chr 20	NC_000020.10:g.4898896T>A
GRCh37.p13 chr 20	NC_000020.10:g.4898896T>C
SLC23A2 RefSeqGene	NG_029959.2:g.97044A>T
SLC23A2 RefSeqGene	NG_029959.2:g.97044A>G

Gene: SLC23A2, solute carrier family 23 member 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC23A2 transcript variant 1	NM_005116.6:c.109-5272A>T	N/A	Intron Variant
SLC23A2 transcript variant 2	NM_203327.2:c.109-5272A>T	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	T=	A	C
GRCh38.p14 chr 20	NC_000020.11:g.4918250=	NC_000020.11:g.4918250T>A	NC_000020.11:g.4918250T>C
GRCh37.p13 chr 20	NC_000020.10:g.4898896=	NC_000020.10:g.4898896T>A	NC_000020.10:g.4898896T>C
SLC23A2 RefSeqGene	NG_029959.2:g.97044=	NG_029959.2:g.97044A>T	NG_029959.2:g.97044A>G
SLC23A2 transcript variant 1	NM_005116.5:c.109-5272=	NM_005116.5:c.109-5272A>T	NM_005116.5:c.109-5272A>G
SLC23A2 transcript variant 1	NM_005116.6:c.109-5272=	NM_005116.6:c.109-5272A>T	NM_005116.6:c.109-5272A>G
SLC23A2 transcript variant 2	NM_203327.1:c.109-5272=	NM_203327.1:c.109-5272A>T	NM_203327.1:c.109-5272A>G
SLC23A2 transcript variant 2	NM_203327.2:c.109-5272=	NM_203327.2:c.109-5272A>T	NM_203327.2:c.109-5272A>G
SLC23A2 transcript variant X1	XM_005260901.1:c.109-5272=	XM_005260901.1:c.109-5272A>T	XM_005260901.1:c.109-5272A>G
SLC23A2 transcript variant X2	XM_005260902.1:c.109-5272=	XM_005260902.1:c.109-5272A>T	XM_005260902.1:c.109-5272A>G
SLC23A2 transcript variant X3	XM_005260903.1:c.109-5272=	XM_005260903.1:c.109-5272A>T	XM_005260903.1:c.109-5272A>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#.

132 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss2551967	Nov 09, 2000 (89)
2	YUSUKE	ss5013611	Aug 28, 2002 (108)
3	SC_SNP	ss8365956	Apr 21, 2003 (114)
4	BCM_SSAHASNP	ss10964116	Jul 11, 2003 (116)
5	WI_SSAHASNP	ss12491198	Jul 11, 2003 (116)
6	CSHL-HAPMAP	ss16897493	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss17697434	Feb 27, 2004 (120)
8	CSHL-HAPMAP	ss20126645	Feb 27, 2004 (120)
9	PERLEGEN	ss24528125	Sep 20, 2004 (123)
10	ABI	ss44229614	Mar 13, 2006 (126)
11	SNP500CANCER	ss48296866	Mar 13, 2006 (126)
12	ILLUMINA	ss66673473	Nov 30, 2006 (127)
13	ILLUMINA	ss67179502	Nov 30, 2006 (127)
14	ILLUMINA	ss67544791	Nov 30, 2006 (127)
15	CSHL-HAPMAP	ss68415326	Jan 12, 2007 (127)
16	ILLUMINA	ss70451081	May 17, 2007 (127)
17	ILLUMINA	ss70657539	May 26, 2008 (130)
18	ILLUMINA	ss71217987	May 17, 2007 (127)
19	ILLUMINA	ss75610160	Dec 06, 2007 (129)
20	KRIBB_YJKIM	ss80731844	Dec 15, 2007 (130)
21	HGSV	ss81220980	Dec 15, 2007 (130)
22	KRIBB_YJKIM	ss83865081	Dec 15, 2007 (130)
23	BCMHGSC_JDW	ss91623579	Mar 24, 2008 (129)
24	BGI	ss106176426	Feb 06, 2009 (130)
25	1000GENOMES	ss111649231	Jan 25, 2009 (130)
26	1000GENOMES	ss115398083	Jan 25, 2009 (130)
27	ILLUMINA-UK	ss117467090	Feb 14, 2009 (130)
28	ILLUMINA	ss121788744	Dec 01, 2009 (131)
29	ENSEMBL	ss138202849	Dec 01, 2009 (131)
30	ILLUMINA	ss153641563	Dec 01, 2009 (131)
31	GMI	ss156112110	Dec 01, 2009 (131)
32	ILLUMINA	ss159311311	Dec 01, 2009 (131)
33	ILLUMINA	ss160430942	Dec 01, 2009 (131)
34	ENSEMBL	ss161328916	Dec 01, 2009 (131)
35	COMPLETE_GENOMICS	ss167724624	Jul 04, 2010 (132)
36	COMPLETE_GENOMICS	ss168947864	Jul 04, 2010 (132)
37	ILLUMINA	ss170756932	Jul 04, 2010 (132)
38	ILLUMINA	ss172768890	Jul 04, 2010 (132)
39	BUSHMAN	ss203816567	Jul 04, 2010 (132)
40	BCM-HGSC-SUB	ss208723296	Jul 04, 2010 (132)
41	1000GENOMES	ss228232130	Jul 14, 2010 (132)
42	1000GENOMES	ss237745800	Jul 15, 2010 (132)
43	1000GENOMES	ss243935883	Jul 15, 2010 (132)
44	BL	ss255451418	May 09, 2011 (134)
45	GMI	ss283284193	May 04, 2012 (137)
46	PJP	ss292569177	May 09, 2011 (134)
47	ILLUMINA	ss480201946	May 04, 2012 (137)
48	ILLUMINA	ss480212293	May 04, 2012 (137)
49	ILLUMINA	ss480940078	Sep 08, 2015 (146)
50	ILLUMINA	ss484899061	May 04, 2012 (137)
51	ILLUMINA	ss536954336	Sep 08, 2015 (146)
52	SSMP	ss661979469	Apr 25, 2013 (138)
53	ILLUMINA	ss778456908	Sep 08, 2015 (146)
54	ILLUMINA	ss782895836	Sep 08, 2015 (146)
55	ILLUMINA	ss783859278	Sep 08, 2015 (146)
56	ILLUMINA	ss825419814	Apr 01, 2015 (144)
57	ILLUMINA	ss832150510	Sep 08, 2015 (146)
58	ILLUMINA	ss832823369	Jul 13, 2019 (153)
59	ILLUMINA	ss833912573	Sep 08, 2015 (146)
60	EVA-GONL	ss994496248	Aug 21, 2014 (142)
61	JMKIDD_LAB	ss1082038779	Aug 21, 2014 (142)
62	1000GENOMES	ss1363908115	Aug 21, 2014 (142)
63	DDI	ss1428982880	Apr 01, 2015 (144)
64	EVA_GENOME_DK	ss1579419426	Apr 01, 2015 (144)
65	EVA_UK10K_ALSPAC	ss1638326396	Apr 01, 2015 (144)
66	EVA_UK10K_TWINSUK	ss1681320429	Apr 01, 2015 (144)
67	EVA_DECODE	ss1698551128	Apr 01, 2015 (144)
68	EVA_SVP	ss1713675905	Apr 01, 2015 (144)
69	ILLUMINA	ss1752390858	Sep 08, 2015 (146)
70	HAMMER_LAB	ss1809403388	Sep 08, 2015 (146)
71	WEILL_CORNELL_DGM	ss1938005888	Feb 12, 2016 (147)
72	GENOMED	ss1969080443	Jul 19, 2016 (147)
73	JJLAB	ss2029780602	Sep 14, 2016 (149)
74	USC_VALOUEV	ss2158334973	Dec 20, 2016 (150)
75	HUMAN_LONGEVITY	ss2241002155	Dec 20, 2016 (150)
76	SYSTEMSBIOZJU	ss2629387667	Nov 08, 2017 (151)
77	ILLUMINA	ss2633771288	Nov 08, 2017 (151)
78	ILLUMINA	ss2635103885	Nov 08, 2017 (151)
79	GRF	ss2704007060	Nov 08, 2017 (151)
80	GNOMAD	ss2964998841	Nov 08, 2017 (151)
81	SWEGEN	ss3017804670	Nov 08, 2017 (151)
82	BIOINF_KMB_FNS_UNIBA	ss3028722662	Nov 08, 2017 (151)
83	CSHL	ss3352399695	Nov 08, 2017 (151)
84	ILLUMINA	ss3628341214	Oct 12, 2018 (152)
85	ILLUMINA	ss3631729353	Oct 12, 2018 (152)
86	ILLUMINA	ss3633242636	Oct 12, 2018 (152)
87	ILLUMINA	ss3633956372	Oct 12, 2018 (152)
88	ILLUMINA	ss3634824516	Oct 12, 2018 (152)
89	ILLUMINA	ss3635641623	Oct 12, 2018 (152)
90	ILLUMINA	ss3636514406	Oct 12, 2018 (152)
91	ILLUMINA	ss3637393687	Oct 12, 2018 (152)
92	ILLUMINA	ss3638332242	Oct 12, 2018 (152)
93	ILLUMINA	ss3639169632	Oct 12, 2018 (152)
94	ILLUMINA	ss3639598819	Oct 12, 2018 (152)
95	ILLUMINA	ss3640531814	Oct 12, 2018 (152)
96	ILLUMINA	ss3641124361	Oct 12, 2018 (152)
97	ILLUMINA	ss3641420541	Oct 12, 2018 (152)
98	ILLUMINA	ss3643295957	Oct 12, 2018 (152)
99	EGCUT_WGS	ss3684518686	Jul 13, 2019 (153)
100	EVA_DECODE	ss3706480576	Jul 13, 2019 (153)
101	ACPOP	ss3743213242	Jul 13, 2019 (153)
102	ILLUMINA	ss3745124406	Jul 13, 2019 (153)
103	EVA	ss3758373393	Jul 13, 2019 (153)
104	ILLUMINA	ss3772620695	Jul 13, 2019 (153)
105	PACBIO	ss3788588546	Jul 13, 2019 (153)
106	PACBIO	ss3793490511	Jul 13, 2019 (153)
107	PACBIO	ss3798377644	Jul 13, 2019 (153)
108	KHV_HUMAN_GENOMES	ss3821544893	Jul 13, 2019 (153)
109	EVA	ss3835566073	Apr 27, 2020 (154)
110	EVA	ss3841406998	Apr 27, 2020 (154)
111	EVA	ss3846914479	Apr 27, 2020 (154)
112	HGDP	ss3847659074	Apr 27, 2020 (154)
113	SGDP_PRJ	ss3888648266	Apr 27, 2020 (154)
114	KRGDB	ss3938833330	Apr 27, 2020 (154)
115	KOGIC	ss3981752594	Apr 27, 2020 (154)
116	EVA	ss3984746222	Apr 26, 2021 (155)
117	EVA	ss3985864564	Apr 26, 2021 (155)
118	EVA	ss4017835399	Apr 26, 2021 (155)
119	TOPMED	ss5080924756	Apr 26, 2021 (155)
120	TOMMO_GENOMICS	ss5228669387	Apr 26, 2021 (155)
121	1000G_HIGH_COVERAGE	ss5307948105	Oct 13, 2022 (156)
122	EVA	ss5315991112	Oct 13, 2022 (156)
123	HUGCELL_USP	ss5500361180	Oct 13, 2022 (156)
124	1000G_HIGH_COVERAGE	ss5613961099	Oct 13, 2022 (156)
125	SANFORD_IMAGENETICS	ss5662784420	Oct 13, 2022 (156)
126	TOMMO_GENOMICS	ss5787609598	Oct 13, 2022 (156)
127	EVA	ss5800014757	Oct 13, 2022 (156)
128	YY_MCH	ss5817781663	Oct 13, 2022 (156)
129	EVA	ss5845389097	Oct 13, 2022 (156)
130	EVA	ss5853050984	Oct 13, 2022 (156)
131	EVA	ss5922515837	Oct 13, 2022 (156)
132	EVA	ss5957683095	Oct 13, 2022 (156)
133	1000Genomes	NC_000020.10 - 4898896	Oct 12, 2018 (152)
134	1000Genomes_30x	NC_000020.11 - 4918250	Oct 13, 2022 (156)
135	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 4898896	Oct 12, 2018 (152)
136	Genetic variation in the Estonian population	NC_000020.10 - 4898896	Oct 12, 2018 (152)
137	The Danish reference pan genome	NC_000020.10 - 4898896	Apr 27, 2020 (154)
138	gnomAD - Genomes	NC_000020.11 - 4918250	Apr 26, 2021 (155)
139	Genome of the Netherlands Release 5	NC_000020.10 - 4898896	Apr 27, 2020 (154)
140	HGDP-CEPH-db Supplement 1	NC_000020.9 - 4846896	Apr 27, 2020 (154)
141	HapMap	NC_000020.11 - 4918250	Apr 27, 2020 (154)
142	KOREAN population from KRGDB	NC_000020.10 - 4898896	Apr 27, 2020 (154)
143	Korean Genome Project	NC_000020.11 - 4918250	Apr 27, 2020 (154)
144	Northern Sweden	NC_000020.10 - 4898896	Jul 13, 2019 (153)
145	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000020.10 - 4898896	Apr 26, 2021 (155)
146	CNV burdens in cranial meningiomas	NC_000020.10 - 4898896	Apr 26, 2021 (155)
147	Qatari	NC_000020.10 - 4898896	Apr 27, 2020 (154)
148	SGDP_PRJ	NC_000020.10 - 4898896	Apr 27, 2020 (154)
149	Siberian	NC_000020.10 - 4898896	Apr 27, 2020 (154)
150	8.3KJPN	NC_000020.10 - 4898896	Apr 26, 2021 (155)
151	14KJPN	NC_000020.11 - 4918250	Oct 13, 2022 (156)
152	TopMed	NC_000020.11 - 4918250	Apr 26, 2021 (155)
153	UK 10K study - Twins	NC_000020.10 - 4898896	Oct 12, 2018 (152)
154	A Vietnamese Genetic Variation Database	NC_000020.10 - 4898896	Jul 13, 2019 (153)
155	ALFA	NC_000020.11 - 4918250	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)
rs3827127	Oct 09, 2002 (108)
rs17340471	Oct 07, 2004 (123)
rs60776515	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
46010724, ss3938833330	NC_000020.10:4898895:T:A	NC_000020.11:4918249:T:A	(self)
336966, ss81220980, ss91623579, ss111649231, ss115398083, ss117467090, ss167724624, ss168947864, ss203816567, ss208723296, ss255451418, ss283284193, ss292569177, ss480201946, ss825419814, ss1698551128, ss1713675905, ss2635103885, ss3639169632, ss3639598819, ss3643295957, ss3847659074	NC_000020.9:4846895:T:C	NC_000020.11:4918249:T:C	(self)
77341974, 42810756, 30256934, 5584365, 19075396, 46010724, 16498107, 1090491, 295789, 20047810, 40665246, 10851327, 86638694, 42810756, 9451000, ss228232130, ss237745800, ss243935883, ss480212293, ss480940078, ss484899061, ss536954336, ss661979469, ss778456908, ss782895836, ss783859278, ss832150510, ss832823369, ss833912573, ss994496248, ss1082038779, ss1363908115, ss1428982880, ss1579419426, ss1638326396, ss1681320429, ss1752390858, ss1809403388, ss1938005888, ss1969080443, ss2029780602, ss2158334973, ss2629387667, ss2633771288, ss2704007060, ss2964998841, ss3017804670, ss3352399695, ss3628341214, ss3631729353, ss3633242636, ss3633956372, ss3634824516, ss3635641623, ss3636514406, ss3637393687, ss3638332242, ss3640531814, ss3641124361, ss3641420541, ss3684518686, ss3743213242, ss3745124406, ss3758373393, ss3772620695, ss3788588546, ss3793490511, ss3798377644, ss3835566073, ss3841406998, ss3888648266, ss3938833330, ss3984746222, ss3985864564, ss4017835399, ss5228669387, ss5315991112, ss5662784420, ss5800014757, ss5845389097, ss5957683095	NC_000020.10:4898895:T:C	NC_000020.11:4918249:T:C	(self)
101487034, 545379466, 2057869, 38130595, 121446702, 356033701, 3533847893, ss2241002155, ss3028722662, ss3706480576, ss3821544893, ss3846914479, ss3981752594, ss5080924756, ss5307948105, ss5500361180, ss5613961099, ss5787609598, ss5817781663, ss5853050984, ss5922515837	NC_000020.11:4918249:T:C	NC_000020.11:4918249:T:C	(self)
ss2551967, ss5013611, ss8365956, ss10964116, ss12491198, ss16897493, ss17697434, ss20126645, ss24528125, ss44229614, ss48296866, ss66673473, ss67179502, ss67544791, ss68415326, ss70451081, ss70657539, ss71217987, ss75610160, ss80731844, ss83865081, ss106176426, ss121788744, ss138202849, ss153641563, ss156112110, ss159311311, ss160430942, ss161328916, ss170756932, ss172768890	NT_011387.8:4838895:T:C	NC_000020.11:4918249:T:C	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs1715364

PMID	Title	Author	Year	Journal
18636124	Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.	Skibola CF et al.	2008	PloS one
26838684	Fruit and vegetable intake and vitamin C transporter gene (SLC23A2) polymorphisms in chronic lymphocytic leukaemia.	Casabonne D et al.	2017	European journal of nutrition

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

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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1715364