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dbSNP Short Genetic Variations

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.

rs884949

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:1329415 (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
C>A / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.222483 (58889/264690, TOPMED)
A=0.303772 (62238/204884, ALFA)
A=0.226992 (31817/140168, GnomAD) (+ 20 more)
A=0.13843 (10894/78696, PAGE_STUDY)
A=0.00018 (5/28258, 14KJPN)
A=0.00018 (3/16760, 8.3KJPN)
A=0.1405 (900/6404, 1000G_30x)
A=0.1400 (701/5008, 1000G)
A=0.2344 (1050/4480, Estonian)
A=0.3155 (1216/3854, ALSPAC)
A=0.3269 (1212/3708, TWINSUK)
A=0.0007 (2/2922, KOREAN)
A=0.1727 (360/2084, HGDP_Stanford)
A=0.1394 (227/1628, HapMap)
A=0.2755 (313/1136, Daghestan)
A=0.330 (329/998, GoNL)
A=0.009 (7/792, PRJEB37584)
A=0.275 (165/600, NorthernSweden)
A=0.315 (68/216, Qatari)
C=0.370 (40/108, SGDP_PRJ)
A=0.39 (30/76, Ancient Sardinia)
A=0.28 (11/40, GENOME_DK)
C=0.2 (1/4, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ADARB2 : 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 209920 C=0.697442 A=0.302558
European Sub 184462 C=0.679370 A=0.320630
African Sub 10822 C=0.90418 A=0.09582
African Others Sub 376 C=0.934 A=0.066
African American Sub 10446 C=0.90312 A=0.09688
Asian Sub 604 C=1.000 A=0.000
East Asian Sub 522 C=1.000 A=0.000
Other Asian Sub 82 C=1.00 A=0.00
Latin American 1 Sub 634 C=0.759 A=0.241
Latin American 2 Sub 1496 C=0.7955 A=0.2045
South Asian Sub 5028 C=0.8103 A=0.1897
Other Sub 6874 C=0.7208 A=0.2792


Help

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 C=0.777517 A=0.222483
Allele Frequency Aggregator Total Global 204884 C=0.696228 A=0.303772
Allele Frequency Aggregator European Sub 181368 C=0.679398 A=0.320602
Allele Frequency Aggregator African Sub 9680 C=0.9031 A=0.0969
Allele Frequency Aggregator Other Sub 6074 C=0.7135 A=0.2865
Allele Frequency Aggregator South Asian Sub 5028 C=0.8103 A=0.1897
Allele Frequency Aggregator Latin American 2 Sub 1496 C=0.7955 A=0.2045
Allele Frequency Aggregator Latin American 1 Sub 634 C=0.759 A=0.241
Allele Frequency Aggregator Asian Sub 604 C=1.000 A=0.000
gnomAD - Genomes Global Study-wide 140168 C=0.773008 A=0.226992
gnomAD - Genomes European Sub 75890 C=0.70397 A=0.29603
gnomAD - Genomes African Sub 42018 C=0.89990 A=0.10010
gnomAD - Genomes American Sub 13658 C=0.75326 A=0.24674
gnomAD - Genomes Ashkenazi Jewish Sub 3320 C=0.6343 A=0.3657
gnomAD - Genomes East Asian Sub 3130 C=0.9981 A=0.0019
gnomAD - Genomes Other Sub 2152 C=0.7421 A=0.2579
The PAGE Study Global Study-wide 78696 C=0.86157 A=0.13843
The PAGE Study AfricanAmerican Sub 32512 C=0.89954 A=0.10046
The PAGE Study Mexican Sub 10810 C=0.82535 A=0.17465
The PAGE Study Asian Sub 8318 C=0.9978 A=0.0022
The PAGE Study PuertoRican Sub 7918 C=0.7417 A=0.2583
The PAGE Study NativeHawaiian Sub 4534 C=0.9118 A=0.0882
The PAGE Study Cuban Sub 4230 C=0.6988 A=0.3012
The PAGE Study Dominican Sub 3828 C=0.7905 A=0.2095
The PAGE Study CentralAmerican Sub 2448 C=0.8207 A=0.1793
The PAGE Study SouthAmerican Sub 1982 C=0.8229 A=0.1771
The PAGE Study NativeAmerican Sub 1260 C=0.7532 A=0.2468
The PAGE Study SouthAsian Sub 856 C=0.883 A=0.117
14KJPN JAPANESE Study-wide 28258 C=0.99982 A=0.00018
8.3KJPN JAPANESE Study-wide 16760 C=0.99982 A=0.00018
1000Genomes_30x Global Study-wide 6404 C=0.8595 A=0.1405
1000Genomes_30x African Sub 1786 C=0.9530 A=0.0470
1000Genomes_30x Europe Sub 1266 C=0.6453 A=0.3547
1000Genomes_30x South Asian Sub 1202 C=0.8677 A=0.1323
1000Genomes_30x East Asian Sub 1170 C=0.9966 A=0.0034
1000Genomes_30x American Sub 980 C=0.792 A=0.208
1000Genomes Global Study-wide 5008 C=0.8600 A=0.1400
1000Genomes African Sub 1322 C=0.9546 A=0.0454
1000Genomes East Asian Sub 1008 C=0.9950 A=0.0050
1000Genomes Europe Sub 1006 C=0.6501 A=0.3499
1000Genomes South Asian Sub 978 C=0.862 A=0.138
1000Genomes American Sub 694 C=0.785 A=0.215
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.7656 A=0.2344
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.6845 A=0.3155
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.6731 A=0.3269
KOREAN population from KRGDB KOREAN Study-wide 2922 C=0.9993 A=0.0007
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 C=0.8273 A=0.1727
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.989 A=0.011
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.737 A=0.263
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.637 A=0.363
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.656 A=0.344
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.967 A=0.033
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.995 A=0.005
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=1.00 A=0.00
HapMap Global Study-wide 1628 C=0.8606 A=0.1394
HapMap African Sub 684 C=0.955 A=0.045
HapMap American Sub 598 C=0.783 A=0.217
HapMap Europe Sub 176 C=0.631 A=0.369
HapMap Asian Sub 170 C=0.994 A=0.006
Genome-wide autozygosity in Daghestan Global Study-wide 1136 C=0.7245 A=0.2755
Genome-wide autozygosity in Daghestan Daghestan Sub 628 C=0.717 A=0.283
Genome-wide autozygosity in Daghestan Near_East Sub 144 C=0.681 A=0.319
Genome-wide autozygosity in Daghestan Central Asia Sub 122 C=0.803 A=0.197
Genome-wide autozygosity in Daghestan Europe Sub 108 C=0.694 A=0.306
Genome-wide autozygosity in Daghestan South Asian Sub 98 C=0.87 A=0.13
Genome-wide autozygosity in Daghestan Caucasus Sub 36 C=0.47 A=0.53
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.670 A=0.330
CNV burdens in cranial meningiomas Global Study-wide 792 C=0.991 A=0.009
CNV burdens in cranial meningiomas CRM Sub 792 C=0.991 A=0.009
Northern Sweden ACPOP Study-wide 600 C=0.725 A=0.275
Qatari Global Study-wide 216 C=0.685 A=0.315
SGDP_PRJ Global Study-wide 108 C=0.370 A=0.630
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 76 C=0.61 A=0.39
The Danish reference pan genome Danish Study-wide 40 C=0.72 A=0.28
Siberian Global Study-wide 4 C=0.2 A=0.8
Help

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.1329415C>A
GRCh38.p14 chr 10 NC_000010.11:g.1329415C>T
GRCh37.p13 chr 10 NC_000010.10:g.1371610C>A
GRCh37.p13 chr 10 NC_000010.10:g.1371610C>T
Gene: ADARB2, adenosine deaminase RNA specific B2 (inactive) (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ADARB2 transcript NM_018702.4:c.1077+33613G…

NM_018702.4:c.1077+33613G>T

N/A Intron Variant
Help

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
Help

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 C= A T
GRCh38.p14 chr 10 NC_000010.11:g.1329415= NC_000010.11:g.1329415C>A NC_000010.11:g.1329415C>T
GRCh37.p13 chr 10 NC_000010.10:g.1371610= NC_000010.10:g.1371610C>A NC_000010.10:g.1371610C>T
ADARB2 transcript NM_018702.3:c.1077+33613= NM_018702.3:c.1077+33613G>T NM_018702.3:c.1077+33613G>A
ADARB2 transcript NM_018702.4:c.1077+33613= NM_018702.4:c.1077+33613G>T NM_018702.4:c.1077+33613G>A
Help

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#.

111 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1312395 Oct 05, 2000 (86)
2 SC_SNP ss15481335 Feb 27, 2004 (120)
3 ABI ss38532867 Mar 14, 2006 (126)
4 ILLUMINA ss66597208 Nov 29, 2006 (127)
5 ILLUMINA ss67887372 Nov 29, 2006 (127)
6 ILLUMINA ss68025550 Nov 29, 2006 (127)
7 CSHL-HAPMAP ss68372508 Jan 12, 2007 (127)
8 ILLUMINA ss70978329 May 24, 2008 (130)
9 ILLUMINA ss71590188 May 16, 2007 (127)
10 ILLUMINA ss74940360 Dec 07, 2007 (129)
11 ILLUMINA ss79286653 Dec 14, 2007 (130)
12 KRIBB_YJKIM ss83593946 Dec 14, 2007 (130)
13 HUMANGENOME_JCVI ss97528119 Feb 04, 2009 (130)
14 1000GENOMES ss109152778 Jan 23, 2009 (130)
15 ILLUMINA ss122933797 Dec 01, 2009 (131)
16 ENSEMBL ss138751446 Dec 01, 2009 (131)
17 ILLUMINA ss154477522 Dec 01, 2009 (131)
18 ILLUMINA ss159651961 Dec 01, 2009 (131)
19 ILLUMINA ss160962630 Dec 01, 2009 (131)
20 ILLUMINA ss172420617 Jul 04, 2010 (132)
21 ILLUMINA ss174766147 Jul 04, 2010 (132)
22 BCM-HGSC-SUB ss207242644 Jul 04, 2010 (132)
23 1000GENOMES ss224517380 Jul 14, 2010 (132)
24 1000GENOMES ss235015912 Jul 15, 2010 (132)
25 BL ss253978858 May 09, 2011 (134)
26 PJP ss290817775 May 09, 2011 (134)
27 ILLUMINA ss481857213 May 04, 2012 (137)
28 ILLUMINA ss482816648 Sep 08, 2015 (146)
29 ILLUMINA ss537570616 Sep 08, 2015 (146)
30 TISHKOFF ss561713930 Apr 25, 2013 (138)
31 SSMP ss656216286 Apr 25, 2013 (138)
32 ILLUMINA ss825617171 Jul 19, 2016 (147)
33 ILLUMINA ss832560386 Sep 08, 2015 (146)
34 ILLUMINA ss833162771 Jul 13, 2019 (153)
35 EVA-GONL ss987108137 Aug 21, 2014 (142)
36 JMKIDD_LAB ss1076694264 Aug 21, 2014 (142)
37 1000GENOMES ss1335956790 Aug 21, 2014 (142)
38 HAMMER_LAB ss1397569736 Sep 08, 2015 (146)
39 DDI ss1426192055 Apr 01, 2015 (144)
40 EVA_GENOME_DK ss1574848660 Apr 01, 2015 (144)
41 EVA_DECODE ss1596754873 Apr 01, 2015 (144)
42 EVA_UK10K_ALSPAC ss1623819162 Apr 01, 2015 (144)
43 EVA_UK10K_TWINSUK ss1666813195 Apr 01, 2015 (144)
44 EVA_SVP ss1713149716 Apr 01, 2015 (144)
45 ILLUMINA ss1751957912 Sep 08, 2015 (146)
46 WEILL_CORNELL_DGM ss1930426572 Feb 12, 2016 (147)
47 ILLUMINA ss1946273933 Feb 12, 2016 (147)
48 ILLUMINA ss1959232466 Feb 12, 2016 (147)
49 GENOMED ss1967036761 Jul 19, 2016 (147)
50 JJLAB ss2025934626 Sep 14, 2016 (149)
51 USC_VALOUEV ss2154175405 Dec 20, 2016 (150)
52 HUMAN_LONGEVITY ss2172020217 Dec 20, 2016 (150)
53 ILLUMINA ss2632662521 Nov 08, 2017 (151)
54 ILLUMINA ss2710700502 Nov 08, 2017 (151)
55 GNOMAD ss2884645422 Nov 08, 2017 (151)
56 SWEGEN ss3005802001 Nov 08, 2017 (151)
57 ILLUMINA ss3021205992 Nov 08, 2017 (151)
58 BIOINF_KMB_FNS_UNIBA ss3026749089 Nov 08, 2017 (151)
59 CSHL ss3348916822 Nov 08, 2017 (151)
60 ILLUMINA ss3625571795 Oct 12, 2018 (152)
61 ILLUMINA ss3626366498 Oct 12, 2018 (152)
62 ILLUMINA ss3633631294 Oct 12, 2018 (152)
63 ILLUMINA ss3634385750 Oct 12, 2018 (152)
64 ILLUMINA ss3635324179 Oct 12, 2018 (152)
65 ILLUMINA ss3636065292 Oct 12, 2018 (152)
66 ILLUMINA ss3637074745 Oct 12, 2018 (152)
67 ILLUMINA ss3637828694 Oct 12, 2018 (152)
68 ILLUMINA ss3638929481 Oct 12, 2018 (152)
69 ILLUMINA ss3639463926 Oct 12, 2018 (152)
70 ILLUMINA ss3640093098 Oct 12, 2018 (152)
71 ILLUMINA ss3640996091 Oct 12, 2018 (152)
72 ILLUMINA ss3641290270 Oct 12, 2018 (152)
73 ILLUMINA ss3642834017 Oct 12, 2018 (152)
74 ILLUMINA ss3644526611 Oct 12, 2018 (152)
75 URBANLAB ss3649268160 Oct 12, 2018 (152)
76 ILLUMINA ss3651552887 Oct 12, 2018 (152)
77 EGCUT_WGS ss3673331232 Jul 13, 2019 (153)
78 EVA_DECODE ss3689117547 Jul 13, 2019 (153)
79 ILLUMINA ss3725128118 Jul 13, 2019 (153)
80 ACPOP ss3736982922 Jul 13, 2019 (153)
81 ILLUMINA ss3744064706 Jul 13, 2019 (153)
82 ILLUMINA ss3744686639 Jul 13, 2019 (153)
83 EVA ss3747641580 Jul 13, 2019 (153)
84 PAGE_CC ss3771536060 Jul 13, 2019 (153)
85 ILLUMINA ss3772187362 Jul 13, 2019 (153)
86 PACBIO ss3786556126 Jul 13, 2019 (153)
87 PACBIO ss3791751002 Jul 13, 2019 (153)
88 PACBIO ss3796632755 Jul 13, 2019 (153)
89 KHV_HUMAN_GENOMES ss3813005534 Jul 13, 2019 (153)
90 EVA ss3831921376 Apr 26, 2020 (154)
91 EVA ss3839489487 Apr 26, 2020 (154)
92 EVA ss3844955018 Apr 26, 2020 (154)
93 HGDP ss3847372038 Apr 26, 2020 (154)
94 SGDP_PRJ ss3873354240 Apr 26, 2020 (154)
95 KRGDB ss3921285323 Apr 26, 2020 (154)
96 EVA ss3984628191 Apr 26, 2021 (155)
97 EVA ss3985451891 Apr 26, 2021 (155)
98 EVA ss4017465641 Apr 26, 2021 (155)
99 TOPMED ss4839878165 Apr 26, 2021 (155)
100 TOMMO_GENOMICS ss5195902523 Apr 26, 2021 (155)
101 1000G_HIGH_COVERAGE ss5282636107 Oct 16, 2022 (156)
102 EVA ss5391085451 Oct 16, 2022 (156)
103 HUGCELL_USP ss5478442909 Oct 16, 2022 (156)
104 1000G_HIGH_COVERAGE ss5575896675 Oct 16, 2022 (156)
105 SANFORD_IMAGENETICS ss5648510976 Oct 16, 2022 (156)
106 TOMMO_GENOMICS ss5740646342 Oct 16, 2022 (156)
107 YY_MCH ss5811119773 Oct 16, 2022 (156)
108 EVA ss5823859011 Oct 16, 2022 (156)
109 EVA ss5847583764 Oct 16, 2022 (156)
110 EVA ss5877416025 Oct 16, 2022 (156)
111 EVA ss5939790481 Oct 16, 2022 (156)
112 1000Genomes NC_000010.10 - 1371610 Oct 12, 2018 (152)
113 1000Genomes_30x NC_000010.11 - 1329415 Oct 16, 2022 (156)
114 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 1371610 Oct 12, 2018 (152)
115 Genome-wide autozygosity in Daghestan NC_000010.9 - 1361610 Apr 26, 2020 (154)
116 Genetic variation in the Estonian population NC_000010.10 - 1371610 Oct 12, 2018 (152)
117 The Danish reference pan genome NC_000010.10 - 1371610 Apr 26, 2020 (154)
118 gnomAD - Genomes NC_000010.11 - 1329415 Apr 26, 2021 (155)
119 Genome of the Netherlands Release 5 NC_000010.10 - 1371610 Apr 26, 2020 (154)
120 HGDP-CEPH-db Supplement 1 NC_000010.9 - 1361610 Apr 26, 2020 (154)
121 HapMap NC_000010.11 - 1329415 Apr 26, 2020 (154)
122 KOREAN population from KRGDB NC_000010.10 - 1371610 Apr 26, 2020 (154)
123 Northern Sweden NC_000010.10 - 1371610 Jul 13, 2019 (153)
124 The PAGE Study NC_000010.11 - 1329415 Jul 13, 2019 (153)
125 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000010.10 - 1371610 Apr 26, 2021 (155)
126 CNV burdens in cranial meningiomas NC_000010.10 - 1371610 Apr 26, 2021 (155)
127 Qatari NC_000010.10 - 1371610 Apr 26, 2020 (154)
128 SGDP_PRJ NC_000010.10 - 1371610 Apr 26, 2020 (154)
129 Siberian NC_000010.10 - 1371610 Apr 26, 2020 (154)
130 8.3KJPN NC_000010.10 - 1371610 Apr 26, 2021 (155)
131 14KJPN NC_000010.11 - 1329415 Oct 16, 2022 (156)
132 TopMed NC_000010.11 - 1329415 Apr 26, 2021 (155)
133 UK 10K study - Twins NC_000010.10 - 1371610 Oct 12, 2018 (152)
134 ALFA NC_000010.11 - 1329415 Apr 26, 2021 (155)
Help

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)
rs57712566 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3638929481, ss3639463926 NC_000010.8:1361609:C:A NC_000010.11:1329414:C:A (self)
41359, 49930, ss109152778, ss207242644, ss253978858, ss290817775, ss825617171, ss1397569736, ss1596754873, ss1713149716, ss3642834017, ss3847372038 NC_000010.9:1361609:C:A NC_000010.11:1329414:C:A (self)
48292370, 26830462, 19069480, 1991858, 11964559, 28462717, 10267787, 677818, 177646, 12468502, 25371220, 6691759, 53871830, 26830462, ss224517380, ss235015912, ss481857213, ss482816648, ss537570616, ss561713930, ss656216286, ss832560386, ss833162771, ss987108137, ss1076694264, ss1335956790, ss1426192055, ss1574848660, ss1623819162, ss1666813195, ss1751957912, ss1930426572, ss1946273933, ss1959232466, ss1967036761, ss2025934626, ss2154175405, ss2632662521, ss2710700502, ss2884645422, ss3005802001, ss3021205992, ss3348916822, ss3625571795, ss3626366498, ss3633631294, ss3634385750, ss3635324179, ss3636065292, ss3637074745, ss3637828694, ss3640093098, ss3640996091, ss3641290270, ss3644526611, ss3651552887, ss3673331232, ss3736982922, ss3744064706, ss3744686639, ss3747641580, ss3772187362, ss3786556126, ss3791751002, ss3796632755, ss3831921376, ss3839489487, ss3873354240, ss3921285323, ss3984628191, ss3985451891, ss4017465641, ss5195902523, ss5391085451, ss5648510976, ss5823859011, ss5847583764, ss5939790481 NC_000010.10:1371609:C:A NC_000010.11:1329414:C:A (self)
63422610, 341249757, 318885, 757529, 74483446, 55423820, 6982347891, ss2172020217, ss3026749089, ss3649268160, ss3689117547, ss3725128118, ss3771536060, ss3813005534, ss3844955018, ss4839878165, ss5282636107, ss5478442909, ss5575896675, ss5740646342, ss5811119773, ss5877416025 NC_000010.11:1329414:C:A NC_000010.11:1329414:C:A (self)
ss1312395, ss38532867, ss66597208, ss67887372, ss68025550, ss68372508, ss70978329, ss71590188, ss74940360, ss79286653, ss83593946, ss97528119, ss122933797, ss138751446, ss154477522, ss159651961, ss160962630, ss172420617, ss174766147 NT_008705.16:1311609:C:A NC_000010.11:1329414:C:A (self)
ss15481335 NT_077567.3:1311609:C:A NC_000010.11:1329414:C:A (self)
ss2172020217 NC_000010.11:1329414:C:T NC_000010.11:1329414:C:T (self)
Help

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

1 citation for rs884949
PMID Title Author Year Journal
20011587 RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans. Sebastiani P et al. 2009 PloS one
Help

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.

Software version is: 2.0.1.post761+d5e8e07