Name: rs4984803
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.

rs4984803

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:1299928 (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: G>A / G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.474857 (125690/264690, TOPMED)
G=0.401894 (97592/242830, ALFA)
G=0.397501 (81518/205076, GENOGRAPHIC) (+ 22 more)
G=0.468174 (65374/139636, GnomAD)
G=0.10946 (3093/28256, 14KJPN)
G=0.11002 (1844/16760, 8.3KJPN)
G=0.4216 (2700/6404, 1000G_30x)
G=0.4111 (2059/5008, 1000G)
G=0.3667 (1642/4478, Estonian)
G=0.4043 (1558/3854, ALSPAC)
G=0.3937 (1460/3708, TWINSUK)
G=0.1010 (296/2930, KOREAN)
G=0.3964 (826/2084, HGDP_Stanford)
G=0.4626 (866/1872, HapMap)
G=0.1108 (203/1832, Korea1K)
G=0.397 (396/998, GoNL)
G=0.095 (75/786, PRJEB37584)
G=0.313 (188/600, NorthernSweden)
G=0.209 (94/450, SGDP_PRJ)
G=0.435 (94/216, Qatari)
G=0.082 (17/208, Vietnamese)
G=0.42 (42/100, Ancient Sardinia)
G=0.20 (11/54, Siberian)
G=0.50 (20/40, GENOME_DK)
A=0.50 (20/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124903624 : 2KB Upstream 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	247866	G=0.403218	A=0.596782, C=0.000000
European	Sub	213390	G=0.391218	A=0.608782, C=0.000000
African	Sub	9120	G=0.6669	A=0.3331, C=0.0000
African Others	Sub	320	G=0.706	A=0.294, C=0.000
African American	Sub	8800	G=0.6655	A=0.3345, C=0.0000
Asian	Sub	828	G=0.101	A=0.899, C=0.000
East Asian	Sub	650	G=0.100	A=0.900, C=0.000
Other Asian	Sub	178	G=0.107	A=0.893, C=0.000
Latin American 1	Sub	988	G=0.452	A=0.548, C=0.000
Latin American 2	Sub	9060	G=0.4466	A=0.5534, C=0.0000
South Asian	Sub	5060	G=0.3686	A=0.6314, C=0.0000
Other	Sub	9420	G=0.4180	A=0.5820, C=0.0000

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	G=0.474857	A=0.525143
Allele Frequency Aggregator	Total	Global	242830	G=0.401894	A=0.598106, C=0.000000
Allele Frequency Aggregator	European	Sub	210296	G=0.390930	A=0.609070, C=0.000000
Allele Frequency Aggregator	Latin American 2	Sub	9060	G=0.4466	A=0.5534, C=0.0000
Allele Frequency Aggregator	Other	Sub	8620	G=0.4171	A=0.5829, C=0.0000
Allele Frequency Aggregator	African	Sub	7978	G=0.6698	A=0.3302, C=0.0000
Allele Frequency Aggregator	South Asian	Sub	5060	G=0.3686	A=0.6314, C=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	988	G=0.452	A=0.548, C=0.000
Allele Frequency Aggregator	Asian	Sub	828	G=0.101	A=0.899, C=0.000
Genographic Project	Global	Study-wide	205076	G=0.397501	A=0.602499, C=0.000000
gnomAD - Genomes	Global	Study-wide	139636	G=0.468174	A=0.531826
gnomAD - Genomes	European	Sub	75686	G=0.38466	A=0.61534
gnomAD - Genomes	African	Sub	41772	G=0.66406	A=0.33594
gnomAD - Genomes	American	Sub	13576	G=0.44431	A=0.55569
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.3868	A=0.6132
gnomAD - Genomes	East Asian	Sub	3128	G=0.0841	A=0.9159
gnomAD - Genomes	Other	Sub	2152	G=0.4377	A=0.5623
14KJPN	JAPANESE	Study-wide	28256	G=0.10946	A=0.89054
8.3KJPN	JAPANESE	Study-wide	16760	G=0.11002	A=0.88998
1000Genomes_30x	Global	Study-wide	6404	G=0.4216	A=0.5784
1000Genomes_30x	African	Sub	1786	G=0.7290	A=0.2710
1000Genomes_30x	Europe	Sub	1266	G=0.3760	A=0.6240
1000Genomes_30x	South Asian	Sub	1202	G=0.3120	A=0.6880
1000Genomes_30x	East Asian	Sub	1170	G=0.0966	A=0.9034
1000Genomes_30x	American	Sub	980	G=0.443	A=0.557
1000Genomes	Global	Study-wide	5008	G=0.4111	A=0.5889
1000Genomes	African	Sub	1322	G=0.7262	A=0.2738
1000Genomes	East Asian	Sub	1008	G=0.1012	A=0.8988
1000Genomes	Europe	Sub	1006	G=0.3767	A=0.6233
1000Genomes	South Asian	Sub	978	G=0.323	A=0.677
1000Genomes	American	Sub	694	G=0.435	A=0.565
Genetic variation in the Estonian population	Estonian	Study-wide	4478	G=0.3667	A=0.6333
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.4043	A=0.5957
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.3937	A=0.6063
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.1010	A=0.8990
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.3964	A=0.6036
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.111	A=0.889
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.379	A=0.621
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.449	A=0.551
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.438	A=0.562
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.723	A=0.277
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.593	A=0.407
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.24	A=0.76
HapMap	Global	Study-wide	1872	G=0.4626	A=0.5374
HapMap	American	Sub	762	G=0.364	A=0.636
HapMap	African	Sub	680	G=0.719	A=0.281
HapMap	Asian	Sub	254	G=0.110	A=0.890
HapMap	Europe	Sub	176	G=0.409	A=0.591
Korean Genome Project	KOREAN	Study-wide	1832	G=0.1108	A=0.8892
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.397	A=0.603
CNV burdens in cranial meningiomas	Global	Study-wide	786	G=0.095	A=0.905
CNV burdens in cranial meningiomas	CRM	Sub	786	G=0.095	A=0.905
Northern Sweden	ACPOP	Study-wide	600	G=0.313	A=0.687
SGDP_PRJ	Global	Study-wide	450	G=0.209	A=0.791
Qatari	Global	Study-wide	216	G=0.435	A=0.565
A Vietnamese Genetic Variation Database	Global	Study-wide	208	G=0.082	A=0.918
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	100	G=0.42	A=0.58
Siberian	Global	Study-wide	54	G=0.20	A=0.80
The Danish reference pan genome	Danish	Study-wide	40	G=0.50	A=0.50

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.1299928G>A
GRCh38.p14 chr 16	NC_000016.10:g.1299928G>C
GRCh37.p13 chr 16	NC_000016.9:g.1349929G>A
GRCh37.p13 chr 16	NC_000016.9:g.1349929G>C

Gene: LOC124903624, uncharacterized LOC124903624 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903624 transcript	XR_007064939.1:n.	N/A	Upstream 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	G=	A	C
GRCh38.p14 chr 16	NC_000016.10:g.1299928=	NC_000016.10:g.1299928G>A	NC_000016.10:g.1299928G>C
GRCh37.p13 chr 16	NC_000016.9:g.1349929=	NC_000016.9:g.1349929G>A	NC_000016.9:g.1349929G>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#.

146 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss6900934	Feb 20, 2003 (111)
2	BCM_SSAHASNP	ss10841678	Jul 11, 2003 (116)
3	CSHL-HAPMAP	ss16710676	Feb 27, 2004 (120)
4	CSHL-HAPMAP	ss20021607	Feb 27, 2004 (120)
5	SSAHASNP	ss21364563	Apr 05, 2004 (121)
6	ABI	ss43902326	Mar 15, 2006 (126)
7	ILLUMINA	ss65798905	Oct 15, 2006 (127)
8	AFFY	ss66513920	Nov 30, 2006 (127)
9	ILLUMINA	ss66620860	Nov 30, 2006 (127)
10	ILLUMINA	ss67408720	Nov 30, 2006 (127)
11	ILLUMINA	ss67774647	Nov 30, 2006 (127)
12	PERLEGEN	ss69335892	May 17, 2007 (127)
13	ILLUMINA	ss70841136	May 26, 2008 (130)
14	ILLUMINA	ss71425007	May 17, 2007 (127)
15	ILLUMINA	ss75432661	Dec 07, 2007 (129)
16	AFFY	ss76336541	Dec 07, 2007 (129)
17	ILLUMINA	ss79205798	Dec 16, 2007 (130)
18	KRIBB_YJKIM	ss84419002	Dec 16, 2007 (130)
19	HGSV	ss84445642	Dec 16, 2007 (130)
20	BCMHGSC_JDW	ss90286781	Mar 24, 2008 (129)
21	HUMANGENOME_JCVI	ss96617601	Feb 06, 2009 (130)
22	BGI	ss106453568	Feb 06, 2009 (130)
23	1000GENOMES	ss109117664	Jan 23, 2009 (130)
24	ILLUMINA	ss122450656	Dec 01, 2009 (131)
25	ENSEMBL	ss136542456	Dec 01, 2009 (131)
26	ILLUMINA	ss154334453	Dec 01, 2009 (131)
27	GMI	ss156976570	Dec 01, 2009 (131)
28	ILLUMINA	ss159510974	Dec 01, 2009 (131)
29	ILLUMINA	ss160735562	Dec 01, 2009 (131)
30	ENSEMBL	ss161757330	Dec 01, 2009 (131)
31	COMPLETE_GENOMICS	ss167633210	Jul 04, 2010 (132)
32	COMPLETE_GENOMICS	ss168857851	Jul 04, 2010 (132)
33	COMPLETE_GENOMICS	ss170827144	Jul 04, 2010 (132)
34	ILLUMINA	ss172006376	Jul 04, 2010 (132)
35	AFFY	ss173305541	Jul 04, 2010 (132)
36	ILLUMINA	ss173902898	Jul 04, 2010 (132)
37	BCM-HGSC-SUB	ss207657439	Jul 04, 2010 (132)
38	1000GENOMES	ss211669845	Jul 14, 2010 (132)
39	1000GENOMES	ss227092343	Jul 14, 2010 (132)
40	1000GENOMES	ss236918023	Jul 15, 2010 (132)
41	1000GENOMES	ss243279260	Jul 15, 2010 (132)
42	BL	ss255429993	May 09, 2011 (134)
43	GMI	ss282403120	May 04, 2012 (137)
44	GMI	ss287018394	Apr 25, 2013 (138)
45	PJP	ss291833057	May 09, 2011 (134)
46	ILLUMINA	ss481125301	May 04, 2012 (137)
47	ILLUMINA	ss481147456	May 04, 2012 (137)
48	ILLUMINA	ss482136359	Sep 08, 2015 (146)
49	ILLUMINA	ss485357737	May 04, 2012 (137)
50	ILLUMINA	ss537302549	Sep 08, 2015 (146)
51	TISHKOFF	ss564717714	Apr 25, 2013 (138)
52	SSMP	ss660464896	Apr 25, 2013 (138)
53	ILLUMINA	ss778927455	Sep 08, 2015 (146)
54	ILLUMINA	ss783124576	Sep 08, 2015 (146)
55	ILLUMINA	ss784081241	Sep 08, 2015 (146)
56	ILLUMINA	ss825536316	Apr 01, 2015 (144)
57	ILLUMINA	ss832383397	Sep 08, 2015 (146)
58	ILLUMINA	ss833022286	Jul 13, 2019 (153)
59	ILLUMINA	ss834388955	Sep 08, 2015 (146)
60	EVA-GONL	ss992186713	Aug 21, 2014 (142)
61	JMKIDD_LAB	ss1080415435	Aug 21, 2014 (142)
62	1000GENOMES	ss1355005043	Aug 21, 2014 (142)
63	DDI	ss1427749155	Apr 01, 2015 (144)
64	EVA_GENOME_DK	ss1577795638	Apr 01, 2015 (144)
65	EVA_UK10K_ALSPAC	ss1633814204	Apr 01, 2015 (144)
66	EVA_UK10K_TWINSUK	ss1676808237	Apr 01, 2015 (144)
67	EVA_DECODE	ss1696218693	Apr 01, 2015 (144)
68	EVA_SVP	ss1713519241	Apr 01, 2015 (144)
69	ILLUMINA	ss1752182799	Sep 08, 2015 (146)
70	HAMMER_LAB	ss1808376861	Sep 08, 2015 (146)
71	WEILL_CORNELL_DGM	ss1935594162	Feb 12, 2016 (147)
72	ILLUMINA	ss1946405650	Feb 12, 2016 (147)
73	ILLUMINA	ss1959649225	Feb 12, 2016 (147)
74	GENOMED	ss1968198318	Jul 19, 2016 (147)
75	JJLAB	ss2028583425	Sep 14, 2016 (149)
76	USC_VALOUEV	ss2156992792	Nov 08, 2017 (151)
77	HUMAN_LONGEVITY	ss2209872437	Dec 20, 2016 (150)
78	SYSTEMSBIOZJU	ss2628785928	Nov 08, 2017 (151)
79	ILLUMINA	ss2633282287	Nov 08, 2017 (151)
80	GRF	ss2701486590	Nov 08, 2017 (151)
81	ILLUMINA	ss2710826015	Nov 08, 2017 (151)
82	GNOMAD	ss2939276886	Nov 08, 2017 (151)
83	SWEGEN	ss3013915986	Nov 08, 2017 (151)
84	ILLUMINA	ss3021673468	Nov 08, 2017 (151)
85	CSHL	ss3351292269	Nov 08, 2017 (151)
86	ILLUMINA	ss3625685042	Oct 12, 2018 (152)
87	ILLUMINA	ss3627456200	Oct 12, 2018 (152)
88	ILLUMINA	ss3631271454	Oct 12, 2018 (152)
89	ILLUMINA	ss3633111144	Oct 12, 2018 (152)
90	ILLUMINA	ss3633816538	Oct 12, 2018 (152)
91	ILLUMINA	ss3634626998	Oct 12, 2018 (152)
92	ILLUMINA	ss3635505095	Oct 12, 2018 (152)
93	ILLUMINA	ss3636317330	Oct 12, 2018 (152)
94	ILLUMINA	ss3637256471	Oct 12, 2018 (152)
95	ILLUMINA	ss3638108530	Oct 12, 2018 (152)
96	ILLUMINA	ss3639066759	Oct 12, 2018 (152)
97	ILLUMINA	ss3639539223	Oct 12, 2018 (152)
98	ILLUMINA	ss3640334318	Oct 12, 2018 (152)
99	ILLUMINA	ss3641066950	Oct 12, 2018 (152)
100	ILLUMINA	ss3641362399	Oct 12, 2018 (152)
101	ILLUMINA	ss3643091001	Oct 12, 2018 (152)
102	ILLUMINA	ss3644658733	Oct 12, 2018 (152)
103	BIOINF_KMB_FNS_UNIBA	ss3645404018	Oct 12, 2018 (152)
104	URBANLAB	ss3650442975	Oct 12, 2018 (152)
105	ILLUMINA	ss3652077274	Oct 12, 2018 (152)
106	EGCUT_WGS	ss3681042085	Jul 13, 2019 (153)
107	EVA_DECODE	ss3698657378	Jul 13, 2019 (153)
108	ILLUMINA	ss3725535101	Jul 13, 2019 (153)
109	ACPOP	ss3741257499	Jul 13, 2019 (153)
110	ILLUMINA	ss3744136973	Jul 13, 2019 (153)
111	ILLUMINA	ss3744927489	Jul 13, 2019 (153)
112	EVA	ss3753569077	Jul 13, 2019 (153)
113	ILLUMINA	ss3772425931	Jul 13, 2019 (153)
114	PACBIO	ss3787955829	Jul 13, 2019 (153)
115	PACBIO	ss3792951814	Jul 13, 2019 (153)
116	PACBIO	ss3797836689	Jul 13, 2019 (153)
117	KHV_HUMAN_GENOMES	ss3818870671	Jul 13, 2019 (153)
118	EVA	ss3834428057	Apr 27, 2020 (154)
119	EVA	ss3840818565	Apr 27, 2020 (154)
120	EVA	ss3846309190	Apr 27, 2020 (154)
121	HGDP	ss3847536604	Apr 27, 2020 (154)
122	SGDP_PRJ	ss3883742896	Apr 27, 2020 (154)
123	KRGDB	ss3933015102	Apr 27, 2020 (154)
124	KOGIC	ss3976936361	Apr 27, 2020 (154)
125	EVA	ss3984708074	Apr 26, 2021 (155)
126	EVA	ss3985740781	Apr 26, 2021 (155)
127	TOPMED	ss5004650737	Apr 26, 2021 (155)
128	TOMMO_GENOMICS	ss5217996195	Apr 26, 2021 (155)
129	1000G_HIGH_COVERAGE	ss5299804776	Oct 16, 2022 (156)
130	GENOGRAPHIC	ss5314567076	Oct 16, 2022 (156)
131	EVA	ss5315816656	Oct 16, 2022 (156)
132	EVA	ss5421720185	Oct 16, 2022 (156)
133	HUGCELL_USP	ss5493371666	Oct 16, 2022 (156)
134	EVA	ss5511541143	Oct 16, 2022 (156)
135	1000G_HIGH_COVERAGE	ss5601875595	Oct 16, 2022 (156)
136	SANFORD_IMAGENETICS	ss5624372152	Oct 16, 2022 (156)
137	SANFORD_IMAGENETICS	ss5658280414	Oct 16, 2022 (156)
138	TOMMO_GENOMICS	ss5772345563	Oct 16, 2022 (156)
139	YY_MCH	ss5815678421	Oct 16, 2022 (156)
140	EVA	ss5845976874	Oct 16, 2022 (156)
141	EVA	ss5847456963	Oct 16, 2022 (156)
142	EVA	ss5851452611	Oct 16, 2022 (156)
143	EVA	ss5897913257	Oct 16, 2022 (156)
144	EVA	ss5949705435	Oct 16, 2022 (156)
145	EVA	ss5979475109	Oct 16, 2022 (156)
146	EVA	ss5980896857	Oct 16, 2022 (156)
147	1000Genomes	NC_000016.9 - 1349929	Oct 12, 2018 (152)
148	1000Genomes_30x	NC_000016.10 - 1299928	Oct 16, 2022 (156)
149	The Avon Longitudinal Study of Parents and Children	NC_000016.9 - 1349929	Oct 12, 2018 (152)
150	Genetic variation in the Estonian population	NC_000016.9 - 1349929	Oct 12, 2018 (152)
151	Genographic Project	NC_000016.10 - 1299928	Oct 16, 2022 (156)
152	The Danish reference pan genome	NC_000016.9 - 1349929	Apr 27, 2020 (154)
153	gnomAD - Genomes	NC_000016.10 - 1299928	Apr 26, 2021 (155)
154	Genome of the Netherlands Release 5	NC_000016.9 - 1349929	Apr 27, 2020 (154)
155	HGDP-CEPH-db Supplement 1	NC_000016.8 - 1289930	Apr 27, 2020 (154)
156	HapMap	NC_000016.10 - 1299928	Apr 27, 2020 (154)
157	KOREAN population from KRGDB	NC_000016.9 - 1349929	Apr 27, 2020 (154)
158	Korean Genome Project	NC_000016.10 - 1299928	Apr 27, 2020 (154)
159	Northern Sweden	NC_000016.9 - 1349929	Jul 13, 2019 (153)
160	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000016.9 - 1349929	Apr 26, 2021 (155)
161	CNV burdens in cranial meningiomas	NC_000016.9 - 1349929	Apr 26, 2021 (155)
162	Qatari	NC_000016.9 - 1349929	Apr 27, 2020 (154)
163	SGDP_PRJ	NC_000016.9 - 1349929	Apr 27, 2020 (154)
164	Siberian	NC_000016.9 - 1349929	Apr 27, 2020 (154)
165	8.3KJPN	NC_000016.9 - 1349929	Apr 26, 2021 (155)
166	14KJPN	NC_000016.10 - 1299928	Oct 16, 2022 (156)
167	TopMed	NC_000016.10 - 1299928	Apr 26, 2021 (155)
168	UK 10K study - Twins	NC_000016.9 - 1349929	Oct 12, 2018 (152)
169	A Vietnamese Genetic Variation Database	NC_000016.9 - 1349929	Jul 13, 2019 (153)
170	ALFA	NC_000016.10 - 1299928	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)
rs61460106	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
214496, ss66513920, ss76336541, ss84445642, ss90286781, ss109117664, ss167633210, ss168857851, ss170827144, ss173305541, ss207657439, ss211669845, ss255429993, ss282403120, ss287018394, ss291833057, ss481125301, ss825536316, ss1696218693, ss1713519241, ss3639066759, ss3639539223, ss3643091001, ss3847536604	NC_000016.8:1289929:G:A	NC_000016.10:1299927:G:A	(self)
68131000, 37833375, 26780333, 4012846, 16880152, 40192496, 14542364, 966708, 257606, 17636084, 35759876, 9509146, 75965502, 37833375, 8410761, ss227092343, ss236918023, ss243279260, ss481147456, ss482136359, ss485357737, ss537302549, ss564717714, ss660464896, ss778927455, ss783124576, ss784081241, ss832383397, ss833022286, ss834388955, ss992186713, ss1080415435, ss1355005043, ss1427749155, ss1577795638, ss1633814204, ss1676808237, ss1752182799, ss1808376861, ss1935594162, ss1946405650, ss1959649225, ss1968198318, ss2028583425, ss2156992792, ss2628785928, ss2633282287, ss2701486590, ss2710826015, ss2939276886, ss3013915986, ss3021673468, ss3351292269, ss3625685042, ss3627456200, ss3631271454, ss3633111144, ss3633816538, ss3634626998, ss3635505095, ss3636317330, ss3637256471, ss3638108530, ss3640334318, ss3641066950, ss3641362399, ss3644658733, ss3652077274, ss3681042085, ss3741257499, ss3744136973, ss3744927489, ss3753569077, ss3772425931, ss3787955829, ss3792951814, ss3797836689, ss3834428057, ss3840818565, ss3883742896, ss3933015102, ss3984708074, ss3985740781, ss5217996195, ss5315816656, ss5421720185, ss5511541143, ss5624372152, ss5658280414, ss5845976874, ss5847456963, ss5949705435, ss5979475109, ss5980896857	NC_000016.9:1349928:G:A	NC_000016.10:1299927:G:A	(self)
89401530, 103036, 480187600, 1333489, 33314362, 106182667, 220196398, 9169503389, ss2209872437, ss3645404018, ss3650442975, ss3698657378, ss3725535101, ss3818870671, ss3846309190, ss3976936361, ss5004650737, ss5299804776, ss5314567076, ss5493371666, ss5601875595, ss5772345563, ss5815678421, ss5851452611, ss5897913257	NC_000016.10:1299927:G:A	NC_000016.10:1299927:G:A	(self)
ss6900934, ss43902326, ss65798905, ss66620860, ss67408720, ss67774647, ss69335892, ss70841136, ss71425007, ss75432661, ss79205798, ss84419002, ss96617601, ss106453568, ss122450656, ss136542456, ss154334453, ss156976570, ss159510974, ss160735562, ss161757330, ss172006376, ss173902898	NT_010393.16:1289928:G:A	NC_000016.10:1299927:G:A	(self)
ss10841678, ss16710676, ss20021607, ss21364563	NT_037887.3:1289929:G:A	NC_000016.10:1299927:G:A	(self)
103036, 9169503389, ss5314567076	NC_000016.10:1299927:G:C	NC_000016.10:1299927:G: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 rs4984803

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

rs4984803