Name: rs859267
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.

rs859267

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:15922707 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.049923 (13214/264690, TOPMED)
C=0.010457 (2532/242142, ALFA)
C=0.07230 (5675/78488, PAGE_STUDY) (+ 19 more)
C=0.02130 (602/28258, 14KJPN)
C=0.01957 (328/16760, 8.3KJPN)
C=0.0472 (302/6404, 1000G_30x)
C=0.0429 (215/5008, 1000G)
C=0.0080 (36/4480, Estonian)
C=0.0080 (31/3854, ALSPAC)
C=0.0062 (23/3708, TWINSUK)
C=0.0239 (70/2930, KOREAN)
C=0.0374 (78/2084, HGDP_Stanford)
C=0.0958 (154/1608, HapMap)
C=0.001 (1/998, GoNL)
C=0.015 (12/792, PRJEB37584)
C=0.007 (4/600, NorthernSweden)
C=0.042 (9/216, Qatari)
C=0.009 (2/216, Vietnamese)
C=0.00 (0/50, Ancient Sardinia)
A=0.40 (16/40, SGDP_PRJ)
A=0.5 (3/6, Siberian)
C=0.5 (3/6, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADORA2B : 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	242142	A=0.989543	C=0.010457, G=0.000000
European	Sub	215750	A=0.993298	C=0.006702, G=0.000000
African	Sub	6842	A=0.9164	C=0.0836, G=0.0000
African Others	Sub	256	A=0.891	C=0.109, G=0.000
African American	Sub	6586	A=0.9174	C=0.0826, G=0.0000
Asian	Sub	3862	A=0.9793	C=0.0207, G=0.0000
East Asian	Sub	3132	A=0.9783	C=0.0217, G=0.0000
Other Asian	Sub	730	A=0.984	C=0.016, G=0.000
Latin American 1	Sub	1028	A=0.9553	C=0.0447, G=0.0000
Latin American 2	Sub	6604	A=0.9659	C=0.0341, G=0.0000
South Asian	Sub	366	A=0.984	C=0.016, G=0.000
Other	Sub	7690	A=0.9796	C=0.0204, G=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	A=0.950077	C=0.049923
Allele Frequency Aggregator	Total	Global	242142	A=0.989543	C=0.010457, G=0.000000
Allele Frequency Aggregator	European	Sub	215750	A=0.993298	C=0.006702, G=0.000000
Allele Frequency Aggregator	Other	Sub	7690	A=0.9796	C=0.0204, G=0.0000
Allele Frequency Aggregator	African	Sub	6842	A=0.9164	C=0.0836, G=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	6604	A=0.9659	C=0.0341, G=0.0000
Allele Frequency Aggregator	Asian	Sub	3862	A=0.9793	C=0.0207, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1028	A=0.9553	C=0.0447, G=0.0000
Allele Frequency Aggregator	South Asian	Sub	366	A=0.984	C=0.016, G=0.000
The PAGE Study	Global	Study-wide	78488	A=0.92770	C=0.07230
The PAGE Study	AfricanAmerican	Sub	32430	A=0.87623	C=0.12377
The PAGE Study	Mexican	Sub	10776	A=0.96566	C=0.03434
The PAGE Study	Asian	Sub	8294	A=0.9778	C=0.0222
The PAGE Study	PuertoRican	Sub	7898	A=0.9607	C=0.0393
The PAGE Study	NativeHawaiian	Sub	4522	A=0.9863	C=0.0137
The PAGE Study	Cuban	Sub	4216	A=0.9675	C=0.0325
The PAGE Study	Dominican	Sub	3818	A=0.9295	C=0.0705
The PAGE Study	CentralAmerican	Sub	2446	A=0.9272	C=0.0728
The PAGE Study	SouthAmerican	Sub	1976	A=0.9443	C=0.0557
The PAGE Study	NativeAmerican	Sub	1256	A=0.9793	C=0.0207
The PAGE Study	SouthAsian	Sub	856	A=0.982	C=0.018
14KJPN	JAPANESE	Study-wide	28258	A=0.97870	C=0.02130
8.3KJPN	JAPANESE	Study-wide	16760	A=0.98043	C=0.01957
1000Genomes_30x	Global	Study-wide	6404	A=0.9528	C=0.0472
1000Genomes_30x	African	Sub	1786	A=0.8606	C=0.1394
1000Genomes_30x	Europe	Sub	1266	A=0.9984	C=0.0016
1000Genomes_30x	South Asian	Sub	1202	A=0.9933	C=0.0067
1000Genomes_30x	East Asian	Sub	1170	A=0.9872	C=0.0128
1000Genomes_30x	American	Sub	980	A=0.971	C=0.029
1000Genomes	Global	Study-wide	5008	A=0.9571	C=0.0429
1000Genomes	African	Sub	1322	A=0.8714	C=0.1286
1000Genomes	East Asian	Sub	1008	A=0.9861	C=0.0139
1000Genomes	Europe	Sub	1006	A=0.9980	C=0.0020
1000Genomes	South Asian	Sub	978	A=0.993	C=0.007
1000Genomes	American	Sub	694	A=0.968	C=0.032
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.9920	C=0.0080
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.9920	C=0.0080
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.9938	C=0.0062
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.9761	C=0.0239
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.9626	C=0.0374
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.972	C=0.028
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.969	C=0.031
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.974	C=0.026
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.997	C=0.003
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.864	C=0.136
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.958	C=0.042
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=1.00	C=0.00
HapMap	Global	Study-wide	1608	A=0.9042	C=0.0958
HapMap	African	Sub	690	A=0.807	C=0.193
HapMap	American	Sub	664	A=0.971	C=0.029
HapMap	Asian	Sub	254	A=0.992	C=0.008
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.999	C=0.001
CNV burdens in cranial meningiomas	Global	Study-wide	792	A=0.985	C=0.015
CNV burdens in cranial meningiomas	CRM	Sub	792	A=0.985	C=0.015
Northern Sweden	ACPOP	Study-wide	600	A=0.993	C=0.007
Qatari	Global	Study-wide	216	A=0.958	C=0.042
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.991	C=0.009
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	50	A=1.00	C=0.00
SGDP_PRJ	Global	Study-wide	40	A=0.40	C=0.60
Siberian	Global	Study-wide	6	A=0.5	C=0.5

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 17	NC_000017.11:g.15922707A>C
GRCh38.p14 chr 17	NC_000017.11:g.15922707A>G
GRCh37.p13 chr 17	NC_000017.10:g.15826021A>C
GRCh37.p13 chr 17	NC_000017.10:g.15826021A>G

Gene: ADORA2B, adenosine A2b receptor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADORA2B transcript	NM_000676.4:c.	N/A	Genic Upstream Transcript Variant
ADORA2B transcript variant X2	XM_047435373.1:c.-377-173… XM_047435373.1:c.-377-17318A>C	N/A	Intron Variant
ADORA2B transcript variant X3	XM_047435374.1:c.-377-173… XM_047435374.1:c.-377-17318A>C	N/A	Intron Variant
ADORA2B transcript variant X4	XM_011523659.4:c.	N/A	Genic Upstream Transcript Variant
ADORA2B transcript variant X6	XM_011523661.3:c.	N/A	Genic Upstream Transcript Variant
ADORA2B transcript variant X1	XM_017024197.3:c.	N/A	Genic Upstream Transcript Variant
ADORA2B transcript variant X5	XM_047435375.1:c.	N/A	Genic 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	A=	C	G
GRCh38.p14 chr 17	NC_000017.11:g.15922707=	NC_000017.11:g.15922707A>C	NC_000017.11:g.15922707A>G
GRCh37.p13 chr 17	NC_000017.10:g.15826021=	NC_000017.10:g.15826021A>C	NC_000017.10:g.15826021A>G
ADORA2B transcript variant X2	XM_047435373.1:c.-377-17318=	XM_047435373.1:c.-377-17318A>C	XM_047435373.1:c.-377-17318A>G
ADORA2B transcript variant X3	XM_047435374.1:c.-377-17318=	XM_047435374.1:c.-377-17318A>C	XM_047435374.1:c.-377-17318A>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#.

94 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss1259027	Oct 05, 2000 (86)
2	SC_JCM	ss2458848	Nov 08, 2000 (89)
3	CSHL-HAPMAP	ss17590356	Feb 27, 2004 (120)
4	ABI	ss40792946	Mar 15, 2006 (126)
5	ILLUMINA	ss68022516	Dec 01, 2006 (127)
6	ILLUMINA	ss71587143	May 18, 2007 (127)
7	ILLUMINA	ss75398731	Dec 07, 2007 (129)
8	HGSV	ss85603629	Dec 15, 2007 (130)
9	KRIBB_YJKIM	ss119370666	Dec 01, 2009 (131)
10	ILLUMINA	ss160958976	Dec 01, 2009 (131)
11	ENSEMBL	ss161824241	Dec 01, 2009 (131)
12	ILLUMINA	ss174752860	Jul 04, 2010 (132)
13	BUSHMAN	ss202294655	Jul 04, 2010 (132)
14	1000GENOMES	ss227485525	Jul 14, 2010 (132)
15	ILLUMINA	ss481812274	May 04, 2012 (137)
16	ILLUMINA	ss481844810	May 04, 2012 (137)
17	ILLUMINA	ss482805674	Sep 08, 2015 (146)
18	ILLUMINA	ss485700814	May 04, 2012 (137)
19	ILLUMINA	ss537566326	Sep 08, 2015 (146)
20	TISHKOFF	ss565194942	Apr 25, 2013 (138)
21	SSMP	ss660986125	Apr 25, 2013 (138)
22	ILLUMINA	ss779000864	Sep 08, 2015 (146)
23	ILLUMINA	ss783295968	Sep 08, 2015 (146)
24	ILLUMINA	ss784248441	Sep 08, 2015 (146)
25	ILLUMINA	ss832557274	Sep 08, 2015 (146)
26	ILLUMINA	ss834463222	Sep 08, 2015 (146)
27	EVA-GONL	ss992966600	Aug 21, 2014 (142)
28	JMKIDD_LAB	ss1080966133	Aug 21, 2014 (142)
29	1000GENOMES	ss1358065571	Aug 21, 2014 (142)
30	EVA_UK10K_ALSPAC	ss1635371519	Apr 01, 2015 (144)
31	EVA_UK10K_TWINSUK	ss1678365552	Apr 01, 2015 (144)
32	EVA_DECODE	ss1697008779	Apr 01, 2015 (144)
33	EVA_SVP	ss1713573591	Apr 01, 2015 (144)
34	ILLUMINA	ss1752216708	Sep 08, 2015 (146)
35	HAMMER_LAB	ss1808724068	Sep 08, 2015 (146)
36	WEILL_CORNELL_DGM	ss1936417537	Feb 12, 2016 (147)
37	ILLUMINA	ss1946432966	Feb 12, 2016 (147)
38	ILLUMINA	ss1959729114	Feb 12, 2016 (147)
39	USC_VALOUEV	ss2157447337	Dec 20, 2016 (150)
40	HUMAN_LONGEVITY	ss2215814805	Dec 20, 2016 (150)
41	ILLUMINA	ss2633381782	Nov 08, 2017 (151)
42	ILLUMINA	ss2633381783	Nov 08, 2017 (151)
43	ILLUMINA	ss2633381784	Nov 08, 2017 (151)
44	GRF	ss2701994465	Nov 08, 2017 (151)
45	ILLUMINA	ss2710845630	Nov 08, 2017 (151)
46	GNOMAD	ss2948133227	Nov 08, 2017 (151)
47	SWEGEN	ss3015263546	Nov 08, 2017 (151)
48	ILLUMINA	ss3021760399	Nov 08, 2017 (151)
49	ILLUMINA	ss3625705781	Oct 12, 2018 (152)
50	ILLUMINA	ss3627637254	Oct 12, 2018 (152)
51	ILLUMINA	ss3631363933	Oct 12, 2018 (152)
52	ILLUMINA	ss3633137354	Oct 12, 2018 (152)
53	ILLUMINA	ss3633844559	Oct 12, 2018 (152)
54	ILLUMINA	ss3634667554	Oct 12, 2018 (152)
55	ILLUMINA	ss3635532443	Oct 12, 2018 (152)
56	ILLUMINA	ss3636357561	Oct 12, 2018 (152)
57	ILLUMINA	ss3637283960	Oct 12, 2018 (152)
58	ILLUMINA	ss3638152255	Oct 12, 2018 (152)
59	ILLUMINA	ss3640374872	Oct 12, 2018 (152)
60	ILLUMINA	ss3643131369	Oct 12, 2018 (152)
61	ILLUMINA	ss3644683150	Oct 12, 2018 (152)
62	ILLUMINA	ss3652173597	Oct 12, 2018 (152)
63	EGCUT_WGS	ss3682225940	Jul 13, 2019 (153)
64	EVA_DECODE	ss3700166982	Jul 13, 2019 (153)
65	EVA_DECODE	ss3700166983	Jul 13, 2019 (153)
66	ILLUMINA	ss3725607296	Jul 13, 2019 (153)
67	ACPOP	ss3741910127	Jul 13, 2019 (153)
68	ILLUMINA	ss3744148284	Jul 13, 2019 (153)
69	ILLUMINA	ss3744967885	Jul 13, 2019 (153)
70	EVA	ss3754501550	Jul 13, 2019 (153)
71	PAGE_CC	ss3771916822	Jul 13, 2019 (153)
72	ILLUMINA	ss3772465880	Jul 13, 2019 (153)
73	KHV_HUMAN_GENOMES	ss3819774673	Jul 13, 2019 (153)
74	HGDP	ss3847560649	Apr 27, 2020 (154)
75	SGDP_PRJ	ss3885429006	Apr 27, 2020 (154)
76	KRGDB	ss3935033075	Apr 27, 2020 (154)
77	EVA	ss3984720998	Apr 26, 2021 (155)
78	EVA	ss3985784428	Apr 26, 2021 (155)
79	TOPMED	ss5030750075	Apr 26, 2021 (155)
80	TOMMO_GENOMICS	ss5221678966	Apr 26, 2021 (155)
81	1000G_HIGH_COVERAGE	ss5302571420	Oct 17, 2022 (156)
82	EVA	ss5315878219	Oct 17, 2022 (156)
83	EVA	ss5426639788	Oct 17, 2022 (156)
84	HUGCELL_USP	ss5495729186	Oct 17, 2022 (156)
85	EVA	ss5511733969	Oct 17, 2022 (156)
86	1000G_HIGH_COVERAGE	ss5605985680	Oct 17, 2022 (156)
87	SANFORD_IMAGENETICS	ss5624393909	Oct 17, 2022 (156)
88	SANFORD_IMAGENETICS	ss5659806901	Oct 17, 2022 (156)
89	TOMMO_GENOMICS	ss5777326472	Oct 17, 2022 (156)
90	YY_MCH	ss5816374005	Oct 17, 2022 (156)
91	EVA	ss5833778956	Oct 17, 2022 (156)
92	EVA	ss5851759613	Oct 17, 2022 (156)
93	EVA	ss5913383746	Oct 17, 2022 (156)
94	EVA	ss5951219176	Oct 17, 2022 (156)
95	1000Genomes	NC_000017.10 - 15826021	Oct 12, 2018 (152)
96	1000Genomes_30x	NC_000017.11 - 15922707	Oct 17, 2022 (156)
97	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 15826021	Oct 12, 2018 (152)
98	Genetic variation in the Estonian population	NC_000017.10 - 15826021	Oct 12, 2018 (152)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502571478 (NC_000017.11:15922706:A:C 6810/140190) Row 502571479 (NC_000017.11:15922706:A:G 4/140208)	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 502571478 (NC_000017.11:15922706:A:C 6810/140190) Row 502571479 (NC_000017.11:15922706:A:G 4/140208)	-	Apr 26, 2021 (155)
101	Genome of the Netherlands Release 5	NC_000017.10 - 15826021	Apr 27, 2020 (154)
102	HGDP-CEPH-db Supplement 1	NC_000017.9 - 15766746	Apr 27, 2020 (154)
103	HapMap	NC_000017.11 - 15922707	Apr 27, 2020 (154)
104	KOREAN population from KRGDB	NC_000017.10 - 15826021	Apr 27, 2020 (154)
105	Northern Sweden	NC_000017.10 - 15826021	Jul 13, 2019 (153)
106	The PAGE Study	NC_000017.11 - 15922707	Jul 13, 2019 (153)
107	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000017.10 - 15826021	Apr 26, 2021 (155)
108	CNV burdens in cranial meningiomas	NC_000017.10 - 15826021	Apr 26, 2021 (155)
109	Qatari	NC_000017.10 - 15826021	Apr 27, 2020 (154)
110	SGDP_PRJ	NC_000017.10 - 15826021	Apr 27, 2020 (154)
111	Siberian	NC_000017.10 - 15826021	Apr 27, 2020 (154)
112	8.3KJPN	NC_000017.10 - 15826021	Apr 26, 2021 (155)
113	14KJPN	NC_000017.11 - 15922707	Oct 17, 2022 (156)
114	TopMed	NC_000017.11 - 15922707	Apr 26, 2021 (155)
115	UK 10K study - Twins	NC_000017.10 - 15826021	Oct 12, 2018 (152)
116	A Vietnamese Genetic Variation Database	NC_000017.10 - 15826021	Jul 13, 2019 (153)
117	ALFA	NC_000017.11 - 15922707	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)
rs60829500	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
238541, ss85603629, ss202294655, ss481812274, ss1697008779, ss1713573591, ss3643131369, ss3847560649	NC_000017.9:15766745:A:C	NC_000017.11:15922706:A:C	(self)
71285965, 39536764, 27964188, 17626159, 42210469, 15194992, 1010355, 270541, 18459459, 37445986, 9963691, 79648273, 39536764, 8759374, ss227485525, ss481844810, ss482805674, ss485700814, ss537566326, ss565194942, ss660986125, ss779000864, ss783295968, ss784248441, ss832557274, ss834463222, ss992966600, ss1080966133, ss1358065571, ss1635371519, ss1678365552, ss1752216708, ss1808724068, ss1936417537, ss1946432966, ss1959729114, ss2157447337, ss2633381782, ss2633381783, ss2633381784, ss2701994465, ss2710845630, ss2948133227, ss3015263546, ss3021760399, ss3625705781, ss3627637254, ss3631363933, ss3633137354, ss3633844559, ss3634667554, ss3635532443, ss3636357561, ss3637283960, ss3638152255, ss3640374872, ss3644683150, ss3652173597, ss3682225940, ss3741910127, ss3744148284, ss3744967885, ss3754501550, ss3772465880, ss3885429006, ss3935033075, ss3984720998, ss3985784428, ss5221678966, ss5315878219, ss5426639788, ss5511733969, ss5624393909, ss5659806901, ss5833778956, ss5951219176	NC_000017.10:15826020:A:C	NC_000017.11:15922706:A:C	(self)
93511615, 1466606, 1138291, 111163576, 246295737, 387372683, ss2215814805, ss3700166982, ss3725607296, ss3771916822, ss3819774673, ss5030750075, ss5302571420, ss5495729186, ss5605985680, ss5777326472, ss5816374005, ss5851759613, ss5913383746	NC_000017.11:15922706:A:C	NC_000017.11:15922706:A:C	(self)
ss17590356	NT_010718.14:14667026:A:C	NC_000017.11:15922706:A:C	(self)
ss1259027, ss2458848, ss40792946, ss68022516, ss71587143, ss75398731, ss119370666, ss160958976, ss161824241, ss174752860	NT_010718.16:15429394:A:C	NC_000017.11:15922706:A:C	(self)
387372683, ss3700166983	NC_000017.11:15922706:A:G	NC_000017.11:15922706:A:G	(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 rs859267

PMID	Title	Author	Year	Journal
22610502	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Kennedy RB et al.	2012	Human genetics

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

rs859267