Name: rs6039763
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.

rs6039763

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:10202869 (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>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.451127 (139789/309866, ALFA)
A=0.449072 (118865/264690, TOPMED)
A=0.459544 (64326/139978, GnomAD) (+ 21 more)
A=0.35902 (28244/78670, PAGE_STUDY)
A=0.22656 (6402/28258, 14KJPN)
A=0.22828 (3826/16760, 8.3KJPN)
A=0.3788 (2426/6404, 1000G_30x)
A=0.3790 (1898/5008, 1000G)
A=0.4828 (2163/4480, Estonian)
G=0.4338 (1672/3854, ALSPAC)
G=0.4113 (1525/3708, TWINSUK)
A=0.2304 (675/2930, KOREAN)
A=0.3685 (768/2084, HGDP_Stanford)
A=0.2298 (421/1832, Korea1K)
A=0.3698 (656/1774, HapMap)
G=0.436 (435/998, GoNL)
A=0.283 (223/788, PRJEB37584)
G=0.418 (251/600, NorthernSweden)
A=0.234 (115/492, SGDP_PRJ)
A=0.454 (98/216, Qatari)
A=0.415 (88/212, Vietnamese)
A=0.30 (15/50, Siberian)
G=0.47 (19/40, GENOME_DK)
A=0.43 (12/28, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SNAP25-AS1 : Intron Variant
Publications: 1 citation
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	314900	A=0.547901	G=0.452099, T=0.000000
European	Sub	275394	A=0.570699	G=0.429301, T=0.000000
African	Sub	9302	A=0.3115	G=0.6885, T=0.0000
African Others	Sub	360	A=0.244	G=0.756, T=0.000
African American	Sub	8942	A=0.3142	G=0.6858, T=0.0000
Asian	Sub	3984	A=0.2816	G=0.7184, T=0.0000
East Asian	Sub	3208	A=0.2559	G=0.7441, T=0.0000
Other Asian	Sub	776	A=0.388	G=0.612, T=0.000
Latin American 1	Sub	1280	A=0.5070	G=0.4930, T=0.0000
Latin American 2	Sub	9362	A=0.3421	G=0.6579, T=0.0000
South Asian	Sub	5232	A=0.4604	G=0.5396, T=0.0000
Other	Sub	10346	A=0.49159	G=0.50841, T=0.00000

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	309866	A=0.548873	G=0.451127, T=0.000000
Allele Frequency Aggregator	European	Sub	272300	A=0.570701	G=0.429299, T=0.000000
Allele Frequency Aggregator	Other	Sub	9546	A=0.4964	G=0.5036, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	9362	A=0.3421	G=0.6579, T=0.0000
Allele Frequency Aggregator	African	Sub	8162	A=0.3128	G=0.6872, T=0.0000
Allele Frequency Aggregator	South Asian	Sub	5232	A=0.4604	G=0.5396, T=0.0000
Allele Frequency Aggregator	Asian	Sub	3984	A=0.2816	G=0.7184, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1280	A=0.5070	G=0.4930, T=0.0000
TopMed	Global	Study-wide	264690	A=0.449072	G=0.550928
gnomAD - Genomes	Global	Study-wide	139978	A=0.459544	G=0.540456
gnomAD - Genomes	European	Sub	75836	A=0.55029	G=0.44971
gnomAD - Genomes	African	Sub	41922	A=0.31070	G=0.68930
gnomAD - Genomes	American	Sub	13622	A=0.42564	G=0.57436
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	A=0.5506	G=0.4494
gnomAD - Genomes	East Asian	Sub	3126	A=0.2933	G=0.7067
gnomAD - Genomes	Other	Sub	2152	A=0.4768	G=0.5232
The PAGE Study	Global	Study-wide	78670	A=0.35902	G=0.64098
The PAGE Study	AfricanAmerican	Sub	32492	A=0.31722	G=0.68278
The PAGE Study	Mexican	Sub	10810	A=0.33719	G=0.66281
The PAGE Study	Asian	Sub	8318	A=0.2567	G=0.7433
The PAGE Study	PuertoRican	Sub	7910	A=0.4343	G=0.5657
The PAGE Study	NativeHawaiian	Sub	4534	A=0.5256	G=0.4744
The PAGE Study	Cuban	Sub	4230	A=0.5300	G=0.4700
The PAGE Study	Dominican	Sub	3828	A=0.4389	G=0.5611
The PAGE Study	CentralAmerican	Sub	2450	A=0.3355	G=0.6645
The PAGE Study	SouthAmerican	Sub	1982	A=0.3350	G=0.6650
The PAGE Study	NativeAmerican	Sub	1260	A=0.4429	G=0.5571
The PAGE Study	SouthAsian	Sub	856	A=0.436	G=0.564
14KJPN	JAPANESE	Study-wide	28258	A=0.22656	G=0.77344
8.3KJPN	JAPANESE	Study-wide	16760	A=0.22828	G=0.77172
1000Genomes_30x	Global	Study-wide	6404	A=0.3788	G=0.6212
1000Genomes_30x	African	Sub	1786	A=0.2721	G=0.7279
1000Genomes_30x	Europe	Sub	1266	A=0.5387	G=0.4613
1000Genomes_30x	South Asian	Sub	1202	A=0.4260	G=0.5740
1000Genomes_30x	East Asian	Sub	1170	A=0.3197	G=0.6803
1000Genomes_30x	American	Sub	980	A=0.380	G=0.620
1000Genomes	Global	Study-wide	5008	A=0.3790	G=0.6210
1000Genomes	African	Sub	1322	A=0.2746	G=0.7254
1000Genomes	East Asian	Sub	1008	A=0.3204	G=0.6796
1000Genomes	Europe	Sub	1006	A=0.5328	G=0.4672
1000Genomes	South Asian	Sub	978	A=0.424	G=0.576
1000Genomes	American	Sub	694	A=0.376	G=0.624
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.4828	G=0.5172
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.5662	G=0.4338
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.5887	G=0.4113
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.2304	C=0.0000, G=0.7696, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.3685	G=0.6315
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.287	G=0.713
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.435	G=0.565
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.489	G=0.511
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.553	G=0.447
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.231	G=0.769
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.093	G=0.907
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.40	G=0.60
Korean Genome Project	KOREAN	Study-wide	1832	A=0.2298	G=0.7702
HapMap	Global	Study-wide	1774	A=0.3698	G=0.6302
HapMap	African	Sub	688	A=0.281	G=0.719
HapMap	American	Sub	660	A=0.432	G=0.568
HapMap	Asian	Sub	250	A=0.332	G=0.668
HapMap	Europe	Sub	176	A=0.540	G=0.460
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.564	G=0.436
CNV burdens in cranial meningiomas	Global	Study-wide	788	A=0.283	G=0.717
CNV burdens in cranial meningiomas	CRM	Sub	788	A=0.283	G=0.717
Northern Sweden	ACPOP	Study-wide	600	A=0.582	G=0.418
SGDP_PRJ	Global	Study-wide	492	A=0.234	G=0.766
Qatari	Global	Study-wide	216	A=0.454	G=0.546
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.415	G=0.585
Siberian	Global	Study-wide	50	A=0.30	G=0.70
The Danish reference pan genome	Danish	Study-wide	40	A=0.53	G=0.47
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	28	A=0.43	G=0.57

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.10202869A>C
GRCh38.p14 chr 20	NC_000020.11:g.10202869A>G
GRCh38.p14 chr 20	NC_000020.11:g.10202869A>T
GRCh37.p13 chr 20	NC_000020.10:g.10183517A>C
GRCh37.p13 chr 20	NC_000020.10:g.10183517A>G
GRCh37.p13 chr 20	NC_000020.10:g.10183517A>T

Gene: SNAP25-AS1, SNAP25 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SNAP25-AS1 transcript	NR_040710.1:n.	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	A=	C	G	T
GRCh38.p14 chr 20	NC_000020.11:g.10202869=	NC_000020.11:g.10202869A>C	NC_000020.11:g.10202869A>G	NC_000020.11:g.10202869A>T
GRCh37.p13 chr 20	NC_000020.10:g.10183517=	NC_000020.10:g.10183517A>C	NC_000020.10:g.10183517A>G	NC_000020.10:g.10183517A>T

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#.

141 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss8348381	Apr 21, 2003 (114)
2	CSHL-HAPMAP	ss17697312	Feb 27, 2004 (120)
3	SSAHASNP	ss21785313	Apr 05, 2004 (121)
4	AFFY	ss66407951	Dec 01, 2006 (127)
5	ILLUMINA	ss66686725	Dec 01, 2006 (127)
6	ILLUMINA	ss67437028	Dec 01, 2006 (127)
7	ILLUMINA	ss67791393	Dec 01, 2006 (127)
8	CSHL-HAPMAP	ss68414770	Jan 12, 2007 (127)
9	ILLUMINA	ss70855521	May 26, 2008 (130)
10	ILLUMINA	ss71441845	May 18, 2007 (127)
11	ILLUMINA	ss75588383	Dec 07, 2007 (129)
12	AFFY	ss76162945	Dec 07, 2007 (129)
13	HGSV	ss78716338	Dec 07, 2007 (129)
14	ILLUMINA	ss79214959	Dec 15, 2007 (130)
15	HGSV	ss81880266	Dec 15, 2007 (130)
16	KRIBB_YJKIM	ss84452356	Dec 15, 2007 (130)
17	HUMANGENOME_JCVI	ss96185237	Feb 06, 2009 (130)
18	BGI	ss106178857	Feb 06, 2009 (130)
19	1000GENOMES	ss111718963	Jan 25, 2009 (130)
20	1000GENOMES	ss113081829	Jan 25, 2009 (130)
21	ILLUMINA-UK	ss117484004	Feb 14, 2009 (130)
22	ILLUMINA	ss122505350	Dec 01, 2009 (131)
23	ENSEMBL	ss133013934	Dec 01, 2009 (131)
24	ILLUMINA	ss154350193	Dec 01, 2009 (131)
25	GMI	ss156161404	Dec 01, 2009 (131)
26	ILLUMINA	ss159526504	Dec 01, 2009 (131)
27	ILLUMINA	ss160759856	Dec 01, 2009 (131)
28	COMPLETE_GENOMICS	ss167807023	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss169078171	Jul 04, 2010 (132)
30	COMPLETE_GENOMICS	ss171896045	Jul 04, 2010 (132)
31	ILLUMINA	ss172086773	Jul 04, 2010 (132)
32	AFFY	ss172681603	Jul 04, 2010 (132)
33	ILLUMINA	ss173968126	Jul 04, 2010 (132)
34	BUSHMAN	ss203830238	Jul 04, 2010 (132)
35	1000GENOMES	ss228255968	Jul 14, 2010 (132)
36	1000GENOMES	ss237762168	Jul 15, 2010 (132)
37	1000GENOMES	ss243948836	Jul 15, 2010 (132)
38	GMI	ss283299591	May 04, 2012 (137)
39	GMI	ss287422514	Apr 25, 2013 (138)
40	PJP	ss292610222	May 09, 2011 (134)
41	ILLUMINA	ss481198864	May 04, 2012 (137)
42	ILLUMINA	ss481221930	May 04, 2012 (137)
43	ILLUMINA	ss482209284	Sep 08, 2015 (146)
44	ILLUMINA	ss485394663	May 04, 2012 (137)
45	ILLUMINA	ss537332832	Sep 08, 2015 (146)
46	TISHKOFF	ss566135087	Apr 25, 2013 (138)
47	SSMP	ss662006106	Apr 25, 2013 (138)
48	ILLUMINA	ss778935204	Aug 21, 2014 (142)
49	ILLUMINA	ss783142852	Aug 21, 2014 (142)
50	ILLUMINA	ss784099017	Aug 21, 2014 (142)
51	ILLUMINA	ss825545477	Apr 01, 2015 (144)
52	ILLUMINA	ss832401943	Apr 01, 2015 (144)
53	ILLUMINA	ss833037764	Aug 21, 2014 (142)
54	ILLUMINA	ss833628592	Aug 21, 2014 (142)
55	ILLUMINA	ss834396856	Aug 21, 2014 (142)
56	EVA-GONL	ss994537727	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1082072355	Aug 21, 2014 (142)
58	1000GENOMES	ss1364060537	Aug 21, 2014 (142)
59	DDI	ss1428995465	Apr 01, 2015 (144)
60	EVA_GENOME_DK	ss1579436591	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1638409966	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1681403999	Apr 01, 2015 (144)
63	EVA_DECODE	ss1698593655	Apr 01, 2015 (144)
64	EVA_SVP	ss1713679591	Apr 01, 2015 (144)
65	ILLUMINA	ss1752375302	Sep 08, 2015 (146)
66	HAMMER_LAB	ss1809422198	Sep 08, 2015 (146)
67	WEILL_CORNELL_DGM	ss1938048214	Feb 12, 2016 (147)
68	ILLUMINA	ss1946547116	Feb 12, 2016 (147)
69	ILLUMINA	ss1959898701	Feb 12, 2016 (147)
70	GENOMED	ss1969090620	Jul 19, 2016 (147)
71	JJLAB	ss2029803314	Sep 14, 2016 (149)
72	USC_VALOUEV	ss2158357091	Dec 20, 2016 (150)
73	HUMAN_LONGEVITY	ss2241317956	Dec 20, 2016 (150)
74	SYSTEMSBIOZJU	ss2629398743	Nov 08, 2017 (151)
75	ILLUMINA	ss2633777133	Nov 08, 2017 (151)
76	GRF	ss2704030326	Nov 08, 2017 (151)
77	ILLUMINA	ss2710935277	Nov 08, 2017 (151)
78	GNOMAD	ss2965420857	Nov 08, 2017 (151)
79	SWEGEN	ss3017866152	Nov 08, 2017 (151)
80	ILLUMINA	ss3022100866	Nov 08, 2017 (151)
81	BIOINF_KMB_FNS_UNIBA	ss3028734668	Nov 08, 2017 (151)
82	CSHL	ss3352418788	Nov 08, 2017 (151)
83	ILLUMINA	ss3625784372	Oct 12, 2018 (152)
84	ILLUMINA	ss3628350936	Oct 12, 2018 (152)
85	ILLUMINA	ss3631734896	Oct 12, 2018 (152)
86	ILLUMINA	ss3633244392	Oct 12, 2018 (152)
87	ILLUMINA	ss3633958191	Oct 12, 2018 (152)
88	ILLUMINA	ss3634826605	Oct 12, 2018 (152)
89	ILLUMINA	ss3635643407	Oct 12, 2018 (152)
90	ILLUMINA	ss3636517012	Oct 12, 2018 (152)
91	ILLUMINA	ss3637395479	Oct 12, 2018 (152)
92	ILLUMINA	ss3638334772	Oct 12, 2018 (152)
93	ILLUMINA	ss3639171104	Oct 12, 2018 (152)
94	ILLUMINA	ss3639599630	Oct 12, 2018 (152)
95	ILLUMINA	ss3640533903	Oct 12, 2018 (152)
96	ILLUMINA	ss3641125165	Oct 12, 2018 (152)
97	ILLUMINA	ss3641421345	Oct 12, 2018 (152)
98	ILLUMINA	ss3643298319	Oct 12, 2018 (152)
99	ILLUMINA	ss3644777467	Oct 12, 2018 (152)
100	URBANLAB	ss3650971125	Oct 12, 2018 (152)
101	ILLUMINA	ss3652555276	Oct 12, 2018 (152)
102	EGCUT_WGS	ss3684583092	Jul 13, 2019 (153)
103	EVA_DECODE	ss3706557566	Jul 13, 2019 (153)
104	ILLUMINA	ss3725900041	Jul 13, 2019 (153)
105	ACPOP	ss3743247971	Jul 13, 2019 (153)
106	ILLUMINA	ss3744194975	Jul 13, 2019 (153)
107	ILLUMINA	ss3745126505	Jul 13, 2019 (153)
108	EVA	ss3758420295	Jul 13, 2019 (153)
109	PAGE_CC	ss3772036554	Jul 13, 2019 (153)
110	ILLUMINA	ss3772622771	Jul 13, 2019 (153)
111	PACBIO	ss3788599336	Jul 13, 2019 (153)
112	PACBIO	ss3793499683	Jul 13, 2019 (153)
113	PACBIO	ss3798386827	Jul 13, 2019 (153)
114	KHV_HUMAN_GENOMES	ss3821594145	Jul 13, 2019 (153)
115	EVA	ss3835587453	Apr 27, 2020 (154)
116	EVA	ss3841418577	Apr 27, 2020 (154)
117	EVA	ss3846926282	Apr 27, 2020 (154)
118	HGDP	ss3847660857	Apr 27, 2020 (154)
119	SGDP_PRJ	ss3888730288	Apr 27, 2020 (154)
120	KRGDB	ss3938919007	Apr 27, 2020 (154)
121	KOGIC	ss3981821089	Apr 27, 2020 (154)
122	EVA	ss3984746981	Apr 27, 2021 (155)
123	EVA	ss3985867499	Apr 27, 2021 (155)
124	TOPMED	ss5082226288	Apr 27, 2021 (155)
125	TOMMO_GENOMICS	ss5228836004	Apr 27, 2021 (155)
126	1000G_HIGH_COVERAGE	ss5308082227	Oct 13, 2022 (156)
127	EVA	ss5315994687	Oct 13, 2022 (156)
128	EVA	ss5436254358	Oct 13, 2022 (156)
129	HUGCELL_USP	ss5500482964	Oct 13, 2022 (156)
130	EVA	ss5512154451	Oct 13, 2022 (156)
131	1000G_HIGH_COVERAGE	ss5614161489	Oct 13, 2022 (156)
132	SANFORD_IMAGENETICS	ss5624480657	Oct 13, 2022 (156)
133	SANFORD_IMAGENETICS	ss5662863169	Oct 13, 2022 (156)
134	TOMMO_GENOMICS	ss5787822835	Oct 13, 2022 (156)
135	EVA	ss5800016261	Oct 13, 2022 (156)
136	YY_MCH	ss5817815314	Oct 13, 2022 (156)
137	EVA	ss5845442916	Oct 13, 2022 (156)
138	EVA	ss5847914373	Oct 13, 2022 (156)
139	EVA	ss5853068464	Oct 13, 2022 (156)
140	EVA	ss5922670432	Oct 13, 2022 (156)
141	EVA	ss5957764508	Oct 13, 2022 (156)
142	1000Genomes	NC_000020.10 - 10183517	Oct 12, 2018 (152)
143	1000Genomes_30x	NC_000020.11 - 10202869	Oct 13, 2022 (156)
144	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 10183517	Oct 12, 2018 (152)
145	Genetic variation in the Estonian population	NC_000020.10 - 10183517	Oct 12, 2018 (152)
146	The Danish reference pan genome	NC_000020.10 - 10183517	Apr 27, 2020 (154)
147	gnomAD - Genomes	NC_000020.11 - 10202869	Apr 27, 2021 (155)
148	Genome of the Netherlands Release 5	NC_000020.10 - 10183517	Apr 27, 2020 (154)
149	HGDP-CEPH-db Supplement 1	NC_000020.9 - 10131517	Apr 27, 2020 (154)
150	HapMap	NC_000020.11 - 10202869	Apr 27, 2020 (154)
151	KOREAN population from KRGDB	NC_000020.10 - 10183517	Apr 27, 2020 (154)
152	Korean Genome Project	NC_000020.11 - 10202869	Apr 27, 2020 (154)
153	Northern Sweden	NC_000020.10 - 10183517	Jul 13, 2019 (153)
154	The PAGE Study	NC_000020.11 - 10202869	Jul 13, 2019 (153)
155	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000020.10 - 10183517	Apr 27, 2021 (155)
156	CNV burdens in cranial meningiomas	NC_000020.10 - 10183517	Apr 27, 2021 (155)
157	Qatari	NC_000020.10 - 10183517	Apr 27, 2020 (154)
158	SGDP_PRJ	NC_000020.10 - 10183517	Apr 27, 2020 (154)
159	Siberian	NC_000020.10 - 10183517	Apr 27, 2020 (154)
160	8.3KJPN	NC_000020.10 - 10183517	Apr 27, 2021 (155)
161	14KJPN	NC_000020.11 - 10202869	Oct 13, 2022 (156)
162	TopMed	NC_000020.11 - 10202869	Apr 27, 2021 (155)
163	UK 10K study - Twins	NC_000020.10 - 10183517	Oct 12, 2018 (152)
164	A Vietnamese Genetic Variation Database	NC_000020.10 - 10183517	Jul 13, 2019 (153)
165	ALFA	NC_000020.11 - 10202869	Apr 27, 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)
rs60463156	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
46096401, ss3938919007	NC_000020.10:10183516:A:C	NC_000020.11:10202868:A:C	(self)
338749, ss78716338, ss81880266, ss111718963, ss113081829, ss117484004, ss160759856, ss167807023, ss169078171, ss171896045, ss203830238, ss283299591, ss287422514, ss292610222, ss481198864, ss825545477, ss1698593655, ss1713679591, ss3639171104, ss3639599630, ss3643298319, ss3847660857	NC_000020.9:10131516:A:G	NC_000020.11:10202868:A:G	(self)
77499855, 42902311, 30321340, 5601530, 19115862, 46096401, 16532836, 1093426, 296548, 20090136, 40747268, 10873445, 86805311, 42902311, 9471500, ss228255968, ss237762168, ss243948836, ss481221930, ss482209284, ss485394663, ss537332832, ss566135087, ss662006106, ss778935204, ss783142852, ss784099017, ss832401943, ss833037764, ss833628592, ss834396856, ss994537727, ss1082072355, ss1364060537, ss1428995465, ss1579436591, ss1638409966, ss1681403999, ss1752375302, ss1809422198, ss1938048214, ss1946547116, ss1959898701, ss1969090620, ss2029803314, ss2158357091, ss2629398743, ss2633777133, ss2704030326, ss2710935277, ss2965420857, ss3017866152, ss3022100866, ss3352418788, ss3625784372, ss3628350936, ss3631734896, ss3633244392, ss3633958191, ss3634826605, ss3635643407, ss3636517012, ss3637395479, ss3638334772, ss3640533903, ss3641125165, ss3641421345, ss3644777467, ss3652555276, ss3684583092, ss3743247971, ss3744194975, ss3745126505, ss3758420295, ss3772622771, ss3788599336, ss3793499683, ss3798386827, ss3835587453, ss3841418577, ss3888730288, ss3938919007, ss3984746981, ss3985867499, ss5228836004, ss5315994687, ss5436254358, ss5512154451, ss5624480657, ss5662863169, ss5800016261, ss5845442916, ss5847914373, ss5957764508	NC_000020.10:10183516:A:G	NC_000020.11:10202868:A:G	(self)
101687424, 546452781, 2070282, 38199090, 1258023, 121659939, 357335233, 6846988617, ss2241317956, ss3028734668, ss3650971125, ss3706557566, ss3725900041, ss3772036554, ss3821594145, ss3846926282, ss3981821089, ss5082226288, ss5308082227, ss5500482964, ss5614161489, ss5787822835, ss5817815314, ss5853068464, ss5922670432	NC_000020.11:10202868:A:G	NC_000020.11:10202868:A:G	(self)
ss8348381, ss17697312, ss21785313, ss66407951, ss66686725, ss67437028, ss67791393, ss68414770, ss70855521, ss71441845, ss75588383, ss76162945, ss79214959, ss84452356, ss96185237, ss106178857, ss122505350, ss133013934, ss154350193, ss156161404, ss159526504, ss172086773, ss172681603, ss173968126	NT_011387.8:10123516:A:G	NC_000020.11:10202868:A:G	(self)
46096401, ss3938919007	NC_000020.10:10183516:A:T	NC_000020.11:10202868:A:T	(self)
6846988617	NC_000020.11:10202868:A:T	NC_000020.11:10202868:A:T	(self)

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

1 citation for rs6039763

PMID	Title	Author	Year	Journal
23648065	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	Low SK et al.	2013	Cancer science

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
Top▲ Help
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

rs6039763