Name: rs2908792
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.

rs2908792

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:53378507 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.439955 (123717/281204, ALFA)
C=0.393729 (104216/264690, TOPMED)
C=0.397456 (55651/140018, GnomAD) (+ 23 more)
C=0.36409 (28654/78700, PAGE_STUDY)
C=0.36110 (10204/28258, 14KJPN)
C=0.35937 (6023/16760, 8.3KJPN)
C=0.4058 (2599/6404, 1000G_30x)
C=0.4077 (2042/5008, 1000G)
C=0.4174 (1870/4480, Estonian)
C=0.4328 (1668/3854, ALSPAC)
C=0.4342 (1610/3708, TWINSUK)
C=0.3741 (1096/2930, KOREAN)
C=0.3968 (827/2084, HGDP_Stanford)
C=0.3695 (699/1892, HapMap)
C=0.3690 (676/1832, Korea1K)
C=0.4727 (537/1136, Daghestan)
C=0.443 (442/998, GoNL)
C=0.421 (332/788, PRJEB37584)
C=0.319 (200/626, Chileans)
C=0.422 (253/600, NorthernSweden)
T=0.312 (108/346, SGDP_PRJ)
C=0.403 (87/216, Qatari)
C=0.429 (91/212, Vietnamese)
T=0.46 (46/100, Ancient Sardinia)
T=0.47 (19/40, GENOME_DK)
T=0.44 (15/34, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC102723373 : Non Coding Transcript 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	286238	T=0.560541	C=0.439459
European	Sub	252742	T=0.554732	C=0.445268
African	Sub	10752	T=0.66360	C=0.33640
African Others	Sub	394	T=0.673	C=0.327
African American	Sub	10358	T=0.66326	C=0.33674
Asian	Sub	3650	T=0.5403	C=0.4597
East Asian	Sub	2916	T=0.6046	C=0.3954
Other Asian	Sub	734	T=0.285	C=0.715
Latin American 1	Sub	852	T=0.545	C=0.455
Latin American 2	Sub	5078	T=0.6772	C=0.3228
South Asian	Sub	5170	T=0.5242	C=0.4758
Other	Sub	7994	T=0.5659	C=0.4341

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
Allele Frequency Aggregator	Total	Global	281204	T=0.560045	C=0.439955
Allele Frequency Aggregator	European	Sub	249648	T=0.554649	C=0.445351
Allele Frequency Aggregator	African	Sub	9612	T=0.6620	C=0.3380
Allele Frequency Aggregator	Other	Sub	7194	T=0.5660	C=0.4340
Allele Frequency Aggregator	South Asian	Sub	5170	T=0.5242	C=0.4758
Allele Frequency Aggregator	Latin American 2	Sub	5078	T=0.6772	C=0.3228
Allele Frequency Aggregator	Asian	Sub	3650	T=0.5403	C=0.4597
Allele Frequency Aggregator	Latin American 1	Sub	852	T=0.545	C=0.455
TopMed	Global	Study-wide	264690	T=0.606271	C=0.393729
gnomAD - Genomes	Global	Study-wide	140018	T=0.602544	C=0.397456
gnomAD - Genomes	European	Sub	75844	T=0.56739	C=0.43261
gnomAD - Genomes	African	Sub	41932	T=0.66546	C=0.33454
gnomAD - Genomes	American	Sub	13642	T=0.62872	C=0.37128
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.5382	C=0.4618
gnomAD - Genomes	East Asian	Sub	3126	T=0.5813	C=0.4187
gnomAD - Genomes	Other	Sub	2150	T=0.5800	C=0.4200
The PAGE Study	Global	Study-wide	78700	T=0.63591	C=0.36409
The PAGE Study	AfricanAmerican	Sub	32514	T=0.65901	C=0.34099
The PAGE Study	Mexican	Sub	10810	T=0.69454	C=0.30546
The PAGE Study	Asian	Sub	8318	T=0.6368	C=0.3632
The PAGE Study	PuertoRican	Sub	7918	T=0.5961	C=0.4039
The PAGE Study	NativeHawaiian	Sub	4534	T=0.4052	C=0.5948
The PAGE Study	Cuban	Sub	4230	T=0.5759	C=0.4241
The PAGE Study	Dominican	Sub	3828	T=0.6306	C=0.3694
The PAGE Study	CentralAmerican	Sub	2450	T=0.7196	C=0.2804
The PAGE Study	SouthAmerican	Sub	1982	T=0.6963	C=0.3037
The PAGE Study	NativeAmerican	Sub	1260	T=0.6389	C=0.3611
The PAGE Study	SouthAsian	Sub	856	T=0.536	C=0.464
14KJPN	JAPANESE	Study-wide	28258	T=0.63890	C=0.36110
8.3KJPN	JAPANESE	Study-wide	16760	T=0.64063	C=0.35937
1000Genomes_30x	Global	Study-wide	6404	T=0.5942	C=0.4058
1000Genomes_30x	African	Sub	1786	T=0.6601	C=0.3399
1000Genomes_30x	Europe	Sub	1266	T=0.5490	C=0.4510
1000Genomes_30x	South Asian	Sub	1202	T=0.5183	C=0.4817
1000Genomes_30x	East Asian	Sub	1170	T=0.5692	C=0.4308
1000Genomes_30x	American	Sub	980	T=0.655	C=0.345
1000Genomes	Global	Study-wide	5008	T=0.5923	C=0.4077
1000Genomes	African	Sub	1322	T=0.6566	C=0.3434
1000Genomes	East Asian	Sub	1008	T=0.5615	C=0.4385
1000Genomes	Europe	Sub	1006	T=0.5586	C=0.4414
1000Genomes	South Asian	Sub	978	T=0.520	C=0.480
1000Genomes	American	Sub	694	T=0.664	C=0.336
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.5826	C=0.4174
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5672	C=0.4328
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5658	C=0.4342
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6259	C=0.3741
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6032	C=0.3968
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.611	C=0.389
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.556	C=0.444
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.509	C=0.491
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.528	C=0.472
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.727	C=0.273
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.977	C=0.023
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.08	C=0.92
HapMap	Global	Study-wide	1892	T=0.6305	C=0.3695
HapMap	American	Sub	770	T=0.606	C=0.394
HapMap	African	Sub	692	T=0.673	C=0.327
HapMap	Asian	Sub	254	T=0.618	C=0.382
HapMap	Europe	Sub	176	T=0.585	C=0.415
Korean Genome Project	KOREAN	Study-wide	1832	T=0.6310	C=0.3690
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	T=0.5273	C=0.4727
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.519	C=0.481
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.569	C=0.431
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.549	C=0.451
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.481	C=0.519
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.53	C=0.47
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.56	C=0.44
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.557	C=0.443
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.579	C=0.421
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.579	C=0.421
Chileans	Chilean	Study-wide	626	T=0.681	C=0.319
Northern Sweden	ACPOP	Study-wide	600	T=0.578	C=0.422
SGDP_PRJ	Global	Study-wide	346	T=0.312	C=0.688
Qatari	Global	Study-wide	216	T=0.597	C=0.403
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.571	C=0.429
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	100	T=0.46	C=0.54
The Danish reference pan genome	Danish	Study-wide	40	T=0.47	C=0.53
Siberian	Global	Study-wide	34	T=0.44	C=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 16	NC_000016.10:g.53378507T>C
GRCh37.p13 chr 16	NC_000016.9:g.53412419T>C

Gene: LOC102723373, uncharacterized LOC102723373 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC102723373 transcript	NR_119378.1:n.401T>C	N/A	Non Coding Transcript 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=	C
GRCh38.p14 chr 16	NC_000016.10:g.53378507=	NC_000016.10:g.53378507T>C
GRCh37.p13 chr 16	NC_000016.9:g.53412419=	NC_000016.9:g.53412419T>C
LOC102723373 transcript	NR_119378.1:n.401=	NR_119378.1:n.401T>C

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#.

134 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss4104185	Nov 05, 2001 (101)
2	PERLEGEN	ss23561066	Sep 20, 2004 (123)
3	AFFY	ss66444951	Dec 02, 2006 (127)
4	ILLUMINA	ss66647503	Dec 02, 2006 (127)
5	ILLUMINA	ss67282649	Dec 02, 2006 (127)
6	ILLUMINA	ss67684949	Dec 02, 2006 (127)
7	PERLEGEN	ss69344359	May 18, 2007 (127)
8	ILLUMINA	ss70761174	May 25, 2008 (130)
9	ILLUMINA	ss71335022	May 18, 2007 (127)
10	ILLUMINA	ss75545355	Dec 05, 2007 (129)
11	AFFY	ss76229380	Dec 05, 2007 (129)
12	ILLUMINA	ss79153500	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss84120903	Dec 15, 2007 (130)
14	BGI	ss106472034	Feb 06, 2009 (130)
15	1000GENOMES	ss109329652	Jan 24, 2009 (130)
16	1000GENOMES	ss115101229	Jan 25, 2009 (130)
17	ILLUMINA-UK	ss118255735	Feb 14, 2009 (130)
18	ILLUMINA	ss122141402	Dec 01, 2009 (131)
19	ENSEMBL	ss136728060	Dec 01, 2009 (131)
20	ILLUMINA	ss154245592	Dec 01, 2009 (131)
21	ILLUMINA	ss159422467	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss169753286	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss171257854	Jul 04, 2010 (132)
24	ILLUMINA	ss171477907	Jul 04, 2010 (132)
25	AFFY	ss172893842	Jul 04, 2010 (132)
26	ILLUMINA	ss173530918	Jul 04, 2010 (132)
27	BUSHMAN	ss201704373	Jul 04, 2010 (132)
28	BCM-HGSC-SUB	ss207636190	Jul 04, 2010 (132)
29	1000GENOMES	ss227246548	Jul 14, 2010 (132)
30	1000GENOMES	ss237028163	Jul 15, 2010 (132)
31	1000GENOMES	ss243366587	Jul 15, 2010 (132)
32	GMI	ss282535068	May 04, 2012 (137)
33	GMI	ss287076697	Apr 25, 2013 (138)
34	ILLUMINA	ss480714624	May 04, 2012 (137)
35	ILLUMINA	ss480730327	May 04, 2012 (137)
36	ILLUMINA	ss485152081	May 04, 2012 (137)
37	ILLUMINA	ss537147892	Sep 08, 2015 (146)
38	TISHKOFF	ss564904990	Apr 25, 2013 (138)
39	SSMP	ss660676666	Apr 25, 2013 (138)
40	ILLUMINA	ss778884252	Aug 21, 2014 (142)
41	ILLUMINA	ss783022314	Aug 21, 2014 (142)
42	ILLUMINA	ss783982210	Aug 21, 2014 (142)
43	ILLUMINA	ss825484018	Jul 19, 2016 (147)
44	ILLUMINA	ss832279843	Apr 01, 2015 (144)
45	ILLUMINA	ss832934109	Aug 21, 2014 (142)
46	ILLUMINA	ss833524939	Aug 21, 2014 (142)
47	ILLUMINA	ss834345291	Aug 21, 2014 (142)
48	EVA-GONL	ss992497666	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1080628744	Aug 21, 2014 (142)
50	1000GENOMES	ss1356282900	Aug 21, 2014 (142)
51	HAMMER_LAB	ss1397715544	Sep 08, 2015 (146)
52	DDI	ss1427849795	Apr 01, 2015 (144)
53	EVA_GENOME_DK	ss1577916900	Apr 01, 2015 (144)
54	EVA_UK10K_ALSPAC	ss1634441038	Apr 01, 2015 (144)
55	EVA_UK10K_TWINSUK	ss1677435071	Apr 01, 2015 (144)
56	EVA_DECODE	ss1696531894	Apr 01, 2015 (144)
57	EVA_SVP	ss1713539594	Apr 01, 2015 (144)
58	ILLUMINA	ss1752194289	Sep 08, 2015 (146)
59	HAMMER_LAB	ss1808516823	Sep 08, 2015 (146)
60	WEILL_CORNELL_DGM	ss1935933731	Feb 12, 2016 (147)
61	ILLUMINA	ss1946414964	Feb 12, 2016 (147)
62	ILLUMINA	ss1959678795	Feb 12, 2016 (147)
63	GENOMED	ss1968262925	Jul 19, 2016 (147)
64	JJLAB	ss2028748941	Sep 14, 2016 (149)
65	USC_VALOUEV	ss2157185138	Dec 20, 2016 (150)
66	HUMAN_LONGEVITY	ss2212235082	Dec 20, 2016 (150)
67	SYSTEMSBIOZJU	ss2628866458	Nov 08, 2017 (151)
68	ILLUMINA	ss2633318635	Nov 08, 2017 (151)
69	ILLUMINA	ss2635064215	Nov 08, 2017 (151)
70	GRF	ss2701708348	Nov 08, 2017 (151)
71	ILLUMINA	ss2710832915	Nov 08, 2017 (151)
72	GNOMAD	ss2943121294	Nov 08, 2017 (151)
73	SWEGEN	ss3014528466	Nov 08, 2017 (151)
74	ILLUMINA	ss3021706345	Nov 08, 2017 (151)
75	BIOINF_KMB_FNS_UNIBA	ss3028193052	Nov 08, 2017 (151)
76	CSHL	ss3351455641	Nov 08, 2017 (151)
77	ILLUMINA	ss3625693060	Oct 12, 2018 (152)
78	ILLUMINA	ss3627524579	Oct 12, 2018 (152)
79	ILLUMINA	ss3631305027	Oct 12, 2018 (152)
80	ILLUMINA	ss3633120792	Oct 12, 2018 (152)
81	ILLUMINA	ss3633826865	Oct 12, 2018 (152)
82	ILLUMINA	ss3634642193	Oct 12, 2018 (152)
83	ILLUMINA	ss3635515169	Oct 12, 2018 (152)
84	ILLUMINA	ss3637266601	Oct 12, 2018 (152)
85	ILLUMINA	ss3638125404	Oct 12, 2018 (152)
86	ILLUMINA	ss3639074050	Oct 12, 2018 (152)
87	ILLUMINA	ss3639543224	Oct 12, 2018 (152)
88	ILLUMINA	ss3640349512	Oct 12, 2018 (152)
89	ILLUMINA	ss3643106623	Oct 12, 2018 (152)
90	ILLUMINA	ss3644668045	Oct 12, 2018 (152)
91	ILLUMINA	ss3652115115	Oct 12, 2018 (152)
92	EGCUT_WGS	ss3681503978	Jul 13, 2019 (153)
93	EVA_DECODE	ss3699280856	Jul 13, 2019 (153)
94	ILLUMINA	ss3725562175	Jul 13, 2019 (153)
95	ACPOP	ss3741518374	Jul 13, 2019 (153)
96	ILLUMINA	ss3744141226	Jul 13, 2019 (153)
97	ILLUMINA	ss3744942610	Jul 13, 2019 (153)
98	EVA	ss3753947486	Jul 13, 2019 (153)
99	PAGE_CC	ss3771879557	Jul 13, 2019 (153)
100	ILLUMINA	ss3772440895	Jul 13, 2019 (153)
101	PACBIO	ss3788042079	Jul 13, 2019 (153)
102	PACBIO	ss3793024343	Jul 13, 2019 (153)
103	PACBIO	ss3797909329	Jul 13, 2019 (153)
104	KHV_HUMAN_GENOMES	ss3819236034	Jul 13, 2019 (153)
105	EVA	ss3834573952	Apr 27, 2020 (154)
106	EVA	ss3840892252	Apr 27, 2020 (154)
107	EVA	ss3846384081	Apr 27, 2020 (154)
108	HGDP	ss3847545265	Apr 27, 2020 (154)
109	SGDP_PRJ	ss3884456579	Apr 27, 2020 (154)
110	KRGDB	ss3933944008	Apr 27, 2020 (154)
111	KOGIC	ss3977607099	Apr 27, 2020 (154)
112	EVA	ss3984712898	Apr 26, 2021 (155)
113	EVA	ss3985757042	Apr 26, 2021 (155)
114	EVA	ss4017736274	Apr 26, 2021 (155)
115	TOPMED	ss5015722510	Apr 26, 2021 (155)
116	TOMMO_GENOMICS	ss5219615505	Apr 26, 2021 (155)
117	EVA	ss5237563923	Apr 26, 2021 (155)
118	1000G_HIGH_COVERAGE	ss5300992814	Oct 17, 2022 (156)
119	EVA	ss5315838099	Oct 17, 2022 (156)
120	EVA	ss5423773302	Oct 17, 2022 (156)
121	HUGCELL_USP	ss5494339209	Oct 17, 2022 (156)
122	EVA	ss5511613100	Oct 17, 2022 (156)
123	1000G_HIGH_COVERAGE	ss5603658902	Oct 17, 2022 (156)
124	SANFORD_IMAGENETICS	ss5624380101	Oct 17, 2022 (156)
125	SANFORD_IMAGENETICS	ss5658922331	Oct 17, 2022 (156)
126	TOMMO_GENOMICS	ss5774638453	Oct 17, 2022 (156)
127	YY_MCH	ss5815980495	Oct 17, 2022 (156)
128	EVA	ss5846421742	Oct 17, 2022 (156)
129	EVA	ss5847462499	Oct 17, 2022 (156)
130	EVA	ss5847771088	Oct 17, 2022 (156)
131	EVA	ss5851569015	Oct 17, 2022 (156)
132	EVA	ss5899136686	Oct 17, 2022 (156)
133	EVA	ss5950313770	Oct 17, 2022 (156)
134	EVA	ss5979485382	Oct 17, 2022 (156)
135	1000Genomes	NC_000016.9 - 53412419	Oct 12, 2018 (152)
136	1000Genomes_30x	NC_000016.10 - 53378507	Oct 17, 2022 (156)
137	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 53412419	Oct 12, 2018 (152)
138	Chileans	NC_000016.9 - 53412419	Apr 27, 2020 (154)
139	Genome-wide autozygosity in Daghestan	NC_000016.8 - 51969920	Apr 27, 2020 (154)
140	Genetic variation in the Estonian population	NC_000016.9 - 53412419	Oct 12, 2018 (152)
141	The Danish reference pan genome	NC_000016.9 - 53412419	Apr 27, 2020 (154)
142	gnomAD - Genomes	NC_000016.10 - 53378507	Apr 26, 2021 (155)
143	Genome of the Netherlands Release 5	NC_000016.9 - 53412419	Apr 27, 2020 (154)
144	HGDP-CEPH-db Supplement 1	NC_000016.8 - 51969920	Apr 27, 2020 (154)
145	HapMap	NC_000016.10 - 53378507	Apr 27, 2020 (154)
146	KOREAN population from KRGDB	NC_000016.9 - 53412419	Apr 27, 2020 (154)
147	Korean Genome Project	NC_000016.10 - 53378507	Apr 27, 2020 (154)
148	Northern Sweden	NC_000016.9 - 53412419	Jul 13, 2019 (153)
149	The PAGE Study	NC_000016.10 - 53378507	Jul 13, 2019 (153)
150	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000016.9 - 53412419	Apr 26, 2021 (155)
151	CNV burdens in cranial meningiomas	NC_000016.9 - 53412419	Apr 26, 2021 (155)
152	Qatari	NC_000016.9 - 53412419	Apr 27, 2020 (154)
153	SGDP_PRJ	NC_000016.9 - 53412419	Apr 27, 2020 (154)
154	Siberian	NC_000016.9 - 53412419	Apr 27, 2020 (154)
155	8.3KJPN	NC_000016.9 - 53412419	Apr 26, 2021 (155)
156	14KJPN	NC_000016.10 - 53378507	Oct 17, 2022 (156)
157	TopMed	NC_000016.10 - 53378507	Apr 26, 2021 (155)
158	UK 10K study - Twins	NC_000016.9 - 53412419	Oct 12, 2018 (152)
159	A Vietnamese Genetic Variation Database	NC_000016.9 - 53412419	Jul 13, 2019 (153)
160	ALFA	NC_000016.10 - 53378507	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)
rs60074528	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
185545, 223157, ss109329652, ss115101229, ss118255735, ss169753286, ss171257854, ss201704373, ss207636190, ss282535068, ss287076697, ss480714624, ss825484018, ss1397715544, ss1696531894, ss1713539594, ss2635064215, ss3639074050, ss3639543224, ss3643106623, ss3847545265	NC_000016.8:51969919:T:C	NC_000016.10:53378506:T:C	(self)
69446422, 38519122, 168213, 27242226, 4129281, 17177626, 41121402, 14803239, 982969, 262433, 17975653, 36473559, 9701492, 77584812, 38519122, 8545442, ss227246548, ss237028163, ss243366587, ss480730327, ss485152081, ss537147892, ss564904990, ss660676666, ss778884252, ss783022314, ss783982210, ss832279843, ss832934109, ss833524939, ss834345291, ss992497666, ss1080628744, ss1356282900, ss1427849795, ss1577916900, ss1634441038, ss1677435071, ss1752194289, ss1808516823, ss1935933731, ss1946414964, ss1959678795, ss1968262925, ss2028748941, ss2157185138, ss2628866458, ss2633318635, ss2701708348, ss2710832915, ss2943121294, ss3014528466, ss3021706345, ss3351455641, ss3625693060, ss3627524579, ss3631305027, ss3633120792, ss3633826865, ss3634642193, ss3635515169, ss3637266601, ss3638125404, ss3640349512, ss3644668045, ss3652115115, ss3681503978, ss3741518374, ss3744141226, ss3744942610, ss3753947486, ss3772440895, ss3788042079, ss3793024343, ss3797909329, ss3834573952, ss3840892252, ss3884456579, ss3933944008, ss3984712898, ss3985757042, ss4017736274, ss5219615505, ss5237563923, ss5315838099, ss5423773302, ss5511613100, ss5624380101, ss5658922331, ss5846421742, ss5847462499, ss5847771088, ss5950313770, ss5979485382	NC_000016.9:53412418:T:C	NC_000016.10:53378506:T:C	(self)
91184837, 489855936, 1383831, 33985100, 1101026, 108475557, 231268171, 13835509575, ss2212235082, ss3028193052, ss3699280856, ss3725562175, ss3771879557, ss3819236034, ss3846384081, ss3977607099, ss5015722510, ss5300992814, ss5494339209, ss5603658902, ss5774638453, ss5815980495, ss5851569015, ss5899136686	NC_000016.10:53378506:T:C	NC_000016.10:53378506:T:C	(self)
ss4104185, ss23561066, ss66444951, ss66647503, ss67282649, ss67684949, ss69344359, ss70761174, ss71335022, ss75545355, ss76229380, ss79153500, ss84120903, ss106472034, ss122141402, ss136728060, ss154245592, ss159422467, ss171477907, ss172893842, ss173530918	NT_010498.15:7026617:T:C	NC_000016.10:53378506:T:C	(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 rs2908792

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2908792