Name: rs6560716
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.

rs6560716

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:1178396 (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 / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.203793 (53942/264690, TOPMED)
T=0.194013 (40546/208986, ALFA)
T=0.197651 (27677/140030, GnomAD) (+ 19 more)
T=0.32348 (9141/28258, 14KJPN)
T=0.32399 (5430/16760, 8.3KJPN)
T=0.2217 (1420/6404, 1000G_30x)
T=0.2246 (1125/5008, 1000G)
T=0.2067 (926/4480, Estonian)
T=0.1783 (687/3854, ALSPAC)
T=0.1826 (677/3708, TWINSUK)
T=0.3608 (1057/2930, KOREAN)
T=0.2011 (419/2084, HGDP_Stanford)
T=0.2370 (448/1890, HapMap)
T=0.3417 (626/1832, Korea1K)
T=0.209 (209/998, GoNL)
T=0.200 (120/600, NorthernSweden)
T=0.173 (93/538, SGDP_PRJ)
T=0.157 (34/216, Qatari)
T=0.238 (51/214, Vietnamese)
T=0.29 (26/90, Ancient Sardinia)
T=0.14 (8/56, Siberian)
T=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADARB2 : 3 Prime UTR 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	209080	T=0.193998	C=0.806002
European	Sub	178910	T=0.191510	C=0.808490
African	Sub	9728	T=0.2131	C=0.7869
African Others	Sub	348	T=0.227	C=0.773
African American	Sub	9380	T=0.2126	C=0.7874
Asian	Sub	702	T=0.264	C=0.736
East Asian	Sub	556	T=0.286	C=0.714
Other Asian	Sub	146	T=0.178	C=0.822
Latin American 1	Sub	844	T=0.152	C=0.848
Latin American 2	Sub	6892	T=0.2330	C=0.7670
South Asian	Sub	5038	T=0.1846	C=0.8154
Other	Sub	6966	T=0.1975	C=0.8025

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=0.203793	C=0.796207
Allele Frequency Aggregator	Total	Global	208986	T=0.194013	C=0.805987
Allele Frequency Aggregator	European	Sub	178834	T=0.191507	C=0.808493
Allele Frequency Aggregator	African	Sub	9728	T=0.2131	C=0.7869
Allele Frequency Aggregator	Other	Sub	6948	T=0.1980	C=0.8020
Allele Frequency Aggregator	Latin American 2	Sub	6892	T=0.2330	C=0.7670
Allele Frequency Aggregator	South Asian	Sub	5038	T=0.1846	C=0.8154
Allele Frequency Aggregator	Latin American 1	Sub	844	T=0.152	C=0.848
Allele Frequency Aggregator	Asian	Sub	702	T=0.264	C=0.736
gnomAD - Genomes	Global	Study-wide	140030	T=0.197651	C=0.802349
gnomAD - Genomes	European	Sub	75896	T=0.19164	C=0.80836
gnomAD - Genomes	African	Sub	41904	T=0.20444	C=0.79556
gnomAD - Genomes	American	Sub	13644	T=0.19562	C=0.80438
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.1746	C=0.8254
gnomAD - Genomes	East Asian	Sub	3118	T=0.2925	C=0.7075
gnomAD - Genomes	Other	Sub	2146	T=0.1883	C=0.8117
14KJPN	JAPANESE	Study-wide	28258	T=0.32348	C=0.67652
8.3KJPN	JAPANESE	Study-wide	16760	T=0.32399	C=0.67601
1000Genomes_30x	Global	Study-wide	6404	T=0.2217	C=0.7783
1000Genomes_30x	African	Sub	1786	T=0.2531	C=0.7469
1000Genomes_30x	Europe	Sub	1266	T=0.1761	C=0.8239
1000Genomes_30x	South Asian	Sub	1202	T=0.1814	C=0.8186
1000Genomes_30x	East Asian	Sub	1170	T=0.3043	C=0.6957
1000Genomes_30x	American	Sub	980	T=0.174	C=0.826
1000Genomes	Global	Study-wide	5008	T=0.2246	C=0.7754
1000Genomes	African	Sub	1322	T=0.2526	C=0.7474
1000Genomes	East Asian	Sub	1008	T=0.2996	C=0.7004
1000Genomes	Europe	Sub	1006	T=0.1799	C=0.8201
1000Genomes	South Asian	Sub	978	T=0.190	C=0.810
1000Genomes	American	Sub	694	T=0.176	C=0.824
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2067	C=0.7933
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.1783	C=0.8217
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.1826	C=0.8174
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3608	A=0.0000, C=0.6392, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.2011	C=0.7989
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.257	C=0.743
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.186	C=0.814
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.231	C=0.769
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.175	C=0.825
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.236	C=0.764
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.125	C=0.875
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.00	C=1.00
HapMap	Global	Study-wide	1890	T=0.2370	C=0.7630
HapMap	American	Sub	768	T=0.234	C=0.766
HapMap	African	Sub	692	T=0.237	C=0.763
HapMap	Asian	Sub	254	T=0.299	C=0.701
HapMap	Europe	Sub	176	T=0.159	C=0.841
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3417	C=0.6583
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.209	C=0.791
Northern Sweden	ACPOP	Study-wide	600	T=0.200	C=0.800
SGDP_PRJ	Global	Study-wide	538	T=0.173	C=0.827
Qatari	Global	Study-wide	216	T=0.157	C=0.843
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.238	C=0.762
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	90	T=0.29	C=0.71
Siberian	Global	Study-wide	56	T=0.14	C=0.86
The Danish reference pan genome	Danish	Study-wide	40	T=0.25	C=0.75

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 10	NC_000010.11:g.1178396T>A
GRCh38.p14 chr 10	NC_000010.11:g.1178396T>C
GRCh38.p14 chr 10	NC_000010.11:g.1178396T>G
GRCh37.p13 chr 10	NC_000010.10:g.1224336T>A
GRCh37.p13 chr 10	NC_000010.10:g.1224336T>C
GRCh37.p13 chr 10	NC_000010.10:g.1224336T>G

Gene: ADARB2, adenosine deaminase RNA specific B2 (inactive) (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADARB2 transcript	NM_018702.4:c.*4797=	N/A	3 Prime UTR 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	G
GRCh38.p14 chr 10	NC_000010.11:g.1178396=	NC_000010.11:g.1178396T>A	NC_000010.11:g.1178396T>C	NC_000010.11:g.1178396T>G
GRCh37.p13 chr 10	NC_000010.10:g.1224336=	NC_000010.10:g.1224336T>A	NC_000010.10:g.1224336T>C	NC_000010.10:g.1224336T>G
ADARB2 transcript	NM_018702.4:c.*4797=	NM_018702.4:c.*4797A>T	NM_018702.4:c.*4797A>G	NM_018702.4:c.*4797A>C
ADARB2 transcript	NM_018702.3:c.*4797=	NM_018702.3:c.*4797A>T	NM_018702.3:c.*4797A>G	NM_018702.3:c.*4797A>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#.

130 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10597707	Jul 11, 2003 (116)
2	WI_SSAHASNP	ss12074133	Jul 11, 2003 (116)
3	CSHL-HAPMAP	ss16494802	Feb 27, 2004 (120)
4	SSAHASNP	ss20698157	Apr 05, 2004 (121)
5	PERLEGEN	ss24146771	Sep 20, 2004 (123)
6	ABI	ss38518675	Mar 15, 2006 (126)
7	ILLUMINA	ss65747266	Oct 16, 2006 (127)
8	ILLUMINA	ss67472187	Dec 01, 2006 (127)
9	ILLUMINA	ss67827473	Dec 01, 2006 (127)
10	ILLUMINA	ss68254139	Dec 12, 2006 (127)
11	PERLEGEN	ss69066660	May 18, 2007 (127)
12	ILLUMINA	ss70873259	May 26, 2008 (130)
13	ILLUMINA	ss71462506	May 18, 2007 (127)
14	ILLUMINA	ss75820479	Dec 07, 2007 (129)
15	HGSV	ss77709670	Dec 07, 2007 (129)
16	HGSV	ss78619120	Dec 07, 2007 (129)
17	HGSV	ss83907463	Dec 15, 2007 (130)
18	KRIBB_YJKIM	ss84504133	Dec 15, 2007 (130)
19	HGSV	ss84758580	Dec 15, 2007 (130)
20	BCMHGSC_JDW	ss88060784	Mar 23, 2008 (129)
21	HUMANGENOME_JCVI	ss97528009	Feb 06, 2009 (130)
22	BGI	ss106649437	Feb 06, 2009 (130)
23	1000GENOMES	ss109151684	Jan 23, 2009 (130)
24	1000GENOMES	ss115232091	Jan 25, 2009 (130)
25	ILLUMINA-UK	ss118969130	Feb 15, 2009 (130)
26	ENSEMBL	ss131633019	Dec 01, 2009 (131)
27	ENSEMBL	ss138792981	Dec 01, 2009 (131)
28	ILLUMINA	ss154368535	Dec 01, 2009 (131)
29	GMI	ss158086661	Dec 01, 2009 (131)
30	ILLUMINA	ss159544642	Dec 01, 2009 (131)
31	ILLUMINA	ss160787071	Dec 01, 2009 (131)
32	COMPLETE_GENOMICS	ss167626172	Jul 04, 2010 (132)
33	COMPLETE_GENOMICS	ss168838553	Jul 04, 2010 (132)
34	COMPLETE_GENOMICS	ss170229861	Jul 04, 2010 (132)
35	ILLUMINA	ss174035212	Jul 04, 2010 (132)
36	BUSHMAN	ss201034095	Jul 04, 2010 (132)
37	BCM-HGSC-SUB	ss207095716	Jul 04, 2010 (132)
38	1000GENOMES	ss224516679	Jul 14, 2010 (132)
39	1000GENOMES	ss235015413	Jul 15, 2010 (132)
40	1000GENOMES	ss241755687	Jul 15, 2010 (132)
41	BL	ss253977498	May 09, 2011 (134)
42	GMI	ss280443439	May 04, 2012 (137)
43	PJP	ss290817516	May 09, 2011 (134)
44	ILLUMINA	ss481283541	May 04, 2012 (137)
45	ILLUMINA	ss481308287	May 04, 2012 (137)
46	ILLUMINA	ss482291160	Sep 08, 2015 (146)
47	ILLUMINA	ss485437030	May 04, 2012 (137)
48	ILLUMINA	ss537364778	Sep 08, 2015 (146)
49	TISHKOFF	ss561713151	Apr 25, 2013 (138)
50	SSMP	ss656215146	Apr 25, 2013 (138)
51	ILLUMINA	ss778572697	Aug 21, 2014 (142)
52	ILLUMINA	ss783163974	Aug 21, 2014 (142)
53	ILLUMINA	ss784119678	Aug 21, 2014 (142)
54	ILLUMINA	ss832423396	Apr 01, 2015 (144)
55	ILLUMINA	ss833055840	Aug 21, 2014 (142)
56	ILLUMINA	ss833646668	Aug 21, 2014 (142)
57	ILLUMINA	ss834029733	Aug 21, 2014 (142)
58	EVA-GONL	ss987106848	Aug 21, 2014 (142)
59	JMKIDD_LAB	ss1076693403	Aug 21, 2014 (142)
60	1000GENOMES	ss1335951569	Aug 21, 2014 (142)
61	DDI	ss1426191640	Apr 01, 2015 (144)
62	EVA_GENOME_DK	ss1574847872	Apr 01, 2015 (144)
63	EVA_DECODE	ss1596753710	Apr 01, 2015 (144)
64	EVA_UK10K_ALSPAC	ss1623816852	Apr 01, 2015 (144)
65	EVA_UK10K_TWINSUK	ss1666810885	Apr 01, 2015 (144)
66	EVA_SVP	ss1713149611	Apr 01, 2015 (144)
67	ILLUMINA	ss1751950992	Sep 08, 2015 (146)
68	HAMMER_LAB	ss1806215829	Sep 08, 2015 (146)
69	WEILL_CORNELL_DGM	ss1930425070	Feb 12, 2016 (147)
70	GENOMED	ss1967036500	Jul 19, 2016 (147)
71	JJLAB	ss2025933943	Sep 14, 2016 (149)
72	USC_VALOUEV	ss2154174661	Dec 20, 2016 (150)
73	HUMAN_LONGEVITY	ss2172010530	Dec 20, 2016 (150)
74	SYSTEMSBIOZJU	ss2627434657	Nov 08, 2017 (151)
75	ILLUMINA	ss2632662338	Nov 08, 2017 (151)
76	GRF	ss2698395183	Nov 08, 2017 (151)
77	GNOMAD	ss2884630035	Nov 08, 2017 (151)
78	AFFY	ss2984903018	Nov 08, 2017 (151)
79	AFFY	ss2985548159	Nov 08, 2017 (151)
80	SWEGEN	ss3005799793	Nov 08, 2017 (151)
81	BIOINF_KMB_FNS_UNIBA	ss3026748777	Nov 08, 2017 (151)
82	CSHL	ss3348916058	Nov 08, 2017 (151)
83	ILLUMINA	ss3626366171	Oct 12, 2018 (152)
84	ILLUMINA	ss3630690599	Oct 12, 2018 (152)
85	ILLUMINA	ss3632934741	Oct 12, 2018 (152)
86	ILLUMINA	ss3633631237	Oct 12, 2018 (152)
87	ILLUMINA	ss3634385672	Oct 12, 2018 (152)
88	ILLUMINA	ss3635324122	Oct 12, 2018 (152)
89	ILLUMINA	ss3636065227	Oct 12, 2018 (152)
90	ILLUMINA	ss3637074688	Oct 12, 2018 (152)
91	ILLUMINA	ss3637828607	Oct 12, 2018 (152)
92	ILLUMINA	ss3638929435	Oct 12, 2018 (152)
93	ILLUMINA	ss3639776343	Oct 12, 2018 (152)
94	ILLUMINA	ss3640093020	Oct 12, 2018 (152)
95	ILLUMINA	ss3642833933	Oct 12, 2018 (152)
96	ILLUMINA	ss3643829342	Oct 12, 2018 (152)
97	URBANLAB	ss3649267770	Oct 12, 2018 (152)
98	ILLUMINA	ss3653672659	Oct 12, 2018 (152)
99	EGCUT_WGS	ss3673329235	Jul 13, 2019 (153)
100	EVA_DECODE	ss3689115126	Jul 13, 2019 (153)
101	ACPOP	ss3736981787	Jul 13, 2019 (153)
102	ILLUMINA	ss3744686562	Jul 13, 2019 (153)
103	EVA	ss3747639957	Jul 13, 2019 (153)
104	ILLUMINA	ss3772187286	Jul 13, 2019 (153)
105	PACBIO	ss3786555699	Jul 13, 2019 (153)
106	PACBIO	ss3791750515	Jul 13, 2019 (153)
107	PACBIO	ss3796632254	Jul 13, 2019 (153)
108	KHV_HUMAN_GENOMES	ss3813004015	Jul 13, 2019 (153)
109	EVA	ss3831920807	Apr 26, 2020 (154)
110	EVA	ss3839489019	Apr 26, 2020 (154)
111	EVA	ss3844954553	Apr 26, 2020 (154)
112	HGDP	ss3847371983	Apr 26, 2020 (154)
113	SGDP_PRJ	ss3873350586	Apr 26, 2020 (154)
114	KRGDB	ss3921281432	Apr 26, 2020 (154)
115	KOGIC	ss3967044195	Apr 26, 2020 (154)
116	EVA	ss3985451802	Apr 26, 2021 (155)
117	EVA	ss4017465559	Apr 26, 2021 (155)
118	TOPMED	ss4839837443	Apr 26, 2021 (155)
119	TOMMO_GENOMICS	ss5195895827	Apr 26, 2021 (155)
120	1000G_HIGH_COVERAGE	ss5282631116	Oct 16, 2022 (156)
121	EVA	ss5315442994	Oct 16, 2022 (156)
122	HUGCELL_USP	ss5478439221	Oct 16, 2022 (156)
123	1000G_HIGH_COVERAGE	ss5575889815	Oct 16, 2022 (156)
124	SANFORD_IMAGENETICS	ss5648508109	Oct 16, 2022 (156)
125	TOMMO_GENOMICS	ss5740636848	Oct 16, 2022 (156)
126	YY_MCH	ss5811118510	Oct 16, 2022 (156)
127	EVA	ss5823857094	Oct 16, 2022 (156)
128	EVA	ss5849397908	Oct 16, 2022 (156)
129	EVA	ss5877411094	Oct 16, 2022 (156)
130	EVA	ss5939788007	Oct 16, 2022 (156)
131	1000Genomes	NC_000010.10 - 1224336	Oct 12, 2018 (152)
132	1000Genomes_30x	NC_000010.11 - 1178396	Oct 16, 2022 (156)
133	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 1224336	Oct 12, 2018 (152)
134	Genetic variation in the Estonian population	NC_000010.10 - 1224336	Oct 12, 2018 (152)
135	The Danish reference pan genome	NC_000010.10 - 1224336	Apr 26, 2020 (154)
136	gnomAD - Genomes	NC_000010.11 - 1178396	Apr 26, 2021 (155)
137	Genome of the Netherlands Release 5	NC_000010.10 - 1224336	Apr 26, 2020 (154)
138	HGDP-CEPH-db Supplement 1	NC_000010.9 - 1214336	Apr 26, 2020 (154)
139	HapMap	NC_000010.11 - 1178396	Apr 26, 2020 (154)
140	KOREAN population from KRGDB	NC_000010.10 - 1224336	Apr 26, 2020 (154)
141	Korean Genome Project	NC_000010.11 - 1178396	Apr 26, 2020 (154)
142	Northern Sweden	NC_000010.10 - 1224336	Jul 13, 2019 (153)
143	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 1224336	Apr 26, 2021 (155)
144	Qatari	NC_000010.10 - 1224336	Apr 26, 2020 (154)
145	SGDP_PRJ	NC_000010.10 - 1224336	Apr 26, 2020 (154)
146	Siberian	NC_000010.10 - 1224336	Apr 26, 2020 (154)
147	8.3KJPN	NC_000010.10 - 1224336	Apr 26, 2021 (155)
148	14KJPN	NC_000010.11 - 1178396	Oct 16, 2022 (156)
149	TopMed	NC_000010.11 - 1178396	Apr 26, 2021 (155)
150	UK 10K study - Twins	NC_000010.10 - 1224336	Oct 12, 2018 (152)
151	A Vietnamese Genetic Variation Database	NC_000010.10 - 1224336	Jul 13, 2019 (153)
152	ALFA	NC_000010.11 - 1178396	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)
rs60454486	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
28458826, ss3921281432	NC_000010.10:1224335:T:A	NC_000010.11:1178395:T:A	(self)
ss77709670, ss78619120, ss83907463, ss84758580, ss3638929435, ss3639776343, ss3643829342	NC_000010.8:1214335:T:C	NC_000010.11:1178395:T:C	(self)
49875, ss88060784, ss109151684, ss115232091, ss118969130, ss160787071, ss167626172, ss168838553, ss170229861, ss201034095, ss207095716, ss253977498, ss280443439, ss290817516, ss481283541, ss1596753710, ss1713149611, ss3642833933, ss3847371983	NC_000010.9:1214335:T:C	NC_000010.11:1178395:T:C	(self)
48286932, 26827906, 19067483, 1991341, 11963355, 28458826, 10266652, 677729, 12467000, 25367566, 6691015, 53865134, 26827906, 5952702, ss224516679, ss235015413, ss241755687, ss481308287, ss482291160, ss485437030, ss537364778, ss561713151, ss656215146, ss778572697, ss783163974, ss784119678, ss832423396, ss833055840, ss833646668, ss834029733, ss987106848, ss1076693403, ss1335951569, ss1426191640, ss1574847872, ss1623816852, ss1666810885, ss1751950992, ss1806215829, ss1930425070, ss1967036500, ss2025933943, ss2154174661, ss2627434657, ss2632662338, ss2698395183, ss2884630035, ss2984903018, ss2985548159, ss3005799793, ss3348916058, ss3626366171, ss3630690599, ss3632934741, ss3633631237, ss3634385672, ss3635324122, ss3636065227, ss3637074688, ss3637828607, ss3640093020, ss3653672659, ss3673329235, ss3736981787, ss3744686562, ss3747639957, ss3772187286, ss3786555699, ss3791750515, ss3796632254, ss3831920807, ss3839489019, ss3873350586, ss3921281432, ss3985451802, ss4017465559, ss5195895827, ss5315442994, ss5648508109, ss5823857094, ss5939788007	NC_000010.10:1224335:T:C	NC_000010.11:1178395:T:C	(self)
63415750, 341212836, 318614, 23422196, 74473952, 55383098, 11530691602, ss2172010530, ss3026748777, ss3649267770, ss3689115126, ss3813004015, ss3844954553, ss3967044195, ss4839837443, ss5282631116, ss5478439221, ss5575889815, ss5740636848, ss5811118510, ss5849397908, ss5877411094	NC_000010.11:1178395:T:C	NC_000010.11:1178395:T:C	(self)
ss24146771, ss38518675, ss65747266, ss67472187, ss67827473, ss68254139, ss69066660, ss70873259, ss71462506, ss75820479, ss84504133, ss97528009, ss106649437, ss131633019, ss138792981, ss154368535, ss158086661, ss159544642, ss174035212	NT_008705.16:1164335:T:C	NC_000010.11:1178395:T:C	(self)
ss10597707, ss12074133	NT_024115.14:1164335:T:C	NC_000010.11:1178395:T:C	(self)
ss16494802, ss20698157	NT_077567.3:1164335:T:C	NC_000010.11:1178395:T:C	(self)
28458826, ss3921281432	NC_000010.10:1224335:T:G	NC_000010.11:1178395:T: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 rs6560716

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.
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

rs6560716