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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.

rs923048

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:2279752 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.392784 (103966/264690, TOPMED)
A=0.293138 (72721/248078, ALFA)
A=0.375978 (52667/140080, GnomAD) (+ 21 more)
A=0.45277 (35623/78678, PAGE_STUDY)
A=0.25104 (7094/28258, 14KJPN)
A=0.25352 (4249/16760, 8.3KJPN)
A=0.4012 (2569/6404, 1000G_30x)
A=0.3906 (1956/5008, 1000G)
A=0.2589 (1160/4480, Estonian)
A=0.2769 (1067/3854, ALSPAC)
A=0.2691 (998/3708, TWINSUK)
A=0.2693 (789/2930, KOREAN)
A=0.3484 (726/2084, HGDP_Stanford)
A=0.4146 (782/1886, HapMap)
A=0.2718 (498/1832, Korea1K)
A=0.247 (247/998, GoNL)
A=0.259 (205/792, PRJEB37584)
A=0.275 (165/600, NorthernSweden)
G=0.393 (125/318, SGDP_PRJ)
A=0.287 (62/216, Qatari)
A=0.290 (62/214, Vietnamese)
A=0.26 (12/46, Ancient Sardinia)
A=0.23 (9/40, GENOME_DK)
G=0.36 (5/14, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 248150 G=0.706891 A=0.293109
European Sub 216054 G=0.725490 A=0.274510
African Sub 10210 G=0.42674 A=0.57326
African Others Sub 350 G=0.366 A=0.634
African American Sub 9860 G=0.4289 A=0.5711
Asian Sub 780 G=0.726 A=0.274
East Asian Sub 634 G=0.732 A=0.268
Other Asian Sub 146 G=0.699 A=0.301
Latin American 1 Sub 842 G=0.632 A=0.368
Latin American 2 Sub 6896 G=0.5792 A=0.4208
South Asian Sub 5042 G=0.7013 A=0.2987
Other Sub 8326 G=0.6828 A=0.3172


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 G=0.607216 A=0.392784
Allele Frequency Aggregator Total Global 248078 G=0.706862 A=0.293138
Allele Frequency Aggregator European Sub 215996 G=0.725476 A=0.274524
Allele Frequency Aggregator African Sub 10210 G=0.42674 A=0.57326
Allele Frequency Aggregator Other Sub 8312 G=0.6824 A=0.3176
Allele Frequency Aggregator Latin American 2 Sub 6896 G=0.5792 A=0.4208
Allele Frequency Aggregator South Asian Sub 5042 G=0.7013 A=0.2987
Allele Frequency Aggregator Latin American 1 Sub 842 G=0.632 A=0.368
Allele Frequency Aggregator Asian Sub 780 G=0.726 A=0.274
gnomAD - Genomes Global Study-wide 140080 G=0.624022 A=0.375978
gnomAD - Genomes European Sub 75868 G=0.72746 A=0.27254
gnomAD - Genomes African Sub 41958 G=0.42547 A=0.57453
gnomAD - Genomes American Sub 13650 G=0.60278 A=0.39722
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.7357 A=0.2643
gnomAD - Genomes East Asian Sub 3130 G=0.7476 A=0.2524
gnomAD - Genomes Other Sub 2152 G=0.6310 A=0.3690
The PAGE Study Global Study-wide 78678 G=0.54723 A=0.45277
The PAGE Study AfricanAmerican Sub 32496 G=0.43408 A=0.56592
The PAGE Study Mexican Sub 10810 G=0.56772 A=0.43228
The PAGE Study Asian Sub 8316 G=0.7520 A=0.2480
The PAGE Study PuertoRican Sub 7918 G=0.5745 A=0.4255
The PAGE Study NativeHawaiian Sub 4534 G=0.7499 A=0.2501
The PAGE Study Cuban Sub 4228 G=0.6391 A=0.3609
The PAGE Study Dominican Sub 3828 G=0.5316 A=0.4684
The PAGE Study CentralAmerican Sub 2450 G=0.5576 A=0.4424
The PAGE Study SouthAmerican Sub 1982 G=0.5474 A=0.4526
The PAGE Study NativeAmerican Sub 1260 G=0.6548 A=0.3452
The PAGE Study SouthAsian Sub 856 G=0.696 A=0.304
14KJPN JAPANESE Study-wide 28258 G=0.74896 A=0.25104
8.3KJPN JAPANESE Study-wide 16760 G=0.74648 A=0.25352
1000Genomes_30x Global Study-wide 6404 G=0.5988 A=0.4012
1000Genomes_30x African Sub 1786 G=0.3835 A=0.6165
1000Genomes_30x Europe Sub 1266 G=0.7180 A=0.2820
1000Genomes_30x South Asian Sub 1202 G=0.6755 A=0.3245
1000Genomes_30x East Asian Sub 1170 G=0.7410 A=0.2590
1000Genomes_30x American Sub 980 G=0.573 A=0.427
1000Genomes Global Study-wide 5008 G=0.6094 A=0.3906
1000Genomes African Sub 1322 G=0.3880 A=0.6120
1000Genomes East Asian Sub 1008 G=0.7440 A=0.2560
1000Genomes Europe Sub 1006 G=0.7207 A=0.2793
1000Genomes South Asian Sub 978 G=0.683 A=0.317
1000Genomes American Sub 694 G=0.571 A=0.429
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7411 A=0.2589
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7231 A=0.2769
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7309 A=0.2691
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.7307 A=0.2693
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.6516 A=0.3484
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.753 A=0.247
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.705 A=0.295
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.703 A=0.297
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.725 A=0.275
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.413 A=0.587
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.449 A=0.551
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.51 A=0.49
HapMap Global Study-wide 1886 G=0.5854 A=0.4146
HapMap American Sub 766 G=0.666 A=0.334
HapMap African Sub 692 G=0.403 A=0.597
HapMap Asian Sub 252 G=0.742 A=0.258
HapMap Europe Sub 176 G=0.727 A=0.273
Korean Genome Project KOREAN Study-wide 1832 G=0.7282 A=0.2718
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.753 A=0.247
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.741 A=0.259
CNV burdens in cranial meningiomas CRM Sub 792 G=0.741 A=0.259
Northern Sweden ACPOP Study-wide 600 G=0.725 A=0.275
SGDP_PRJ Global Study-wide 318 G=0.393 A=0.607
Qatari Global Study-wide 216 G=0.713 A=0.287
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.710 A=0.290
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 46 G=0.74 A=0.26
The Danish reference pan genome Danish Study-wide 40 G=0.78 A=0.23
Siberian Global Study-wide 14 G=0.36 A=0.64
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 5 NC_000005.10:g.2279752G>A
GRCh37.p13 chr 5 NC_000005.9:g.2279866G>A
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 G= A
GRCh38.p14 chr 5 NC_000005.10:g.2279752= NC_000005.10:g.2279752G>A
GRCh37.p13 chr 5 NC_000005.9:g.2279866= NC_000005.9:g.2279866G>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#.

137 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1359993 Oct 05, 2000 (86)
2 SC_JCM ss3672021 Sep 28, 2001 (100)
3 PERLEGEN ss23742133 Sep 20, 2004 (123)
4 ABI ss44605132 Mar 13, 2006 (126)
5 ILLUMINA ss65720884 Oct 15, 2006 (127)
6 ILLUMINA ss66854269 Nov 30, 2006 (127)
7 ILLUMINA ss67895932 Nov 30, 2006 (127)
8 ILLUMINA ss68030337 Nov 30, 2006 (127)
9 PERLEGEN ss68924209 May 17, 2007 (127)
10 ILLUMINA ss71594987 May 17, 2007 (127)
11 ILLUMINA ss75870784 Dec 07, 2007 (129)
12 ILLUMINA ss79289821 Dec 14, 2007 (130)
13 KRIBB_YJKIM ss83613599 Dec 14, 2007 (130)
14 HGSV ss84968100 Dec 14, 2007 (130)
15 ILLUMINA ss98237388 May 24, 2008 (130)
16 BGI ss105900504 Feb 04, 2009 (130)
17 1000GENOMES ss111307023 Jan 25, 2009 (130)
18 ILLUMINA ss120243078 Dec 01, 2009 (131)
19 ILLUMINA ss122952702 Dec 01, 2009 (131)
20 ILLUMINA ss154481982 Dec 01, 2009 (131)
21 ILLUMINA ss159656392 Dec 01, 2009 (131)
22 ILLUMINA ss160968501 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss161950680 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss164049333 Jul 04, 2010 (132)
25 ILLUMINA ss172433781 Jul 04, 2010 (132)
26 ILLUMINA ss174786352 Jul 04, 2010 (132)
27 BUSHMAN ss199779596 Jul 04, 2010 (132)
28 BCM-HGSC-SUB ss206889617 Jul 04, 2010 (132)
29 1000GENOMES ss221472332 Jul 14, 2010 (132)
30 1000GENOMES ss232796483 Jul 14, 2010 (132)
31 1000GENOMES ss240000247 Jul 15, 2010 (132)
32 ILLUMINA ss244256903 Jul 04, 2010 (132)
33 BL ss253159583 May 09, 2011 (134)
34 GMI ss278137033 May 04, 2012 (137)
35 ILLUMINA ss481844744 May 04, 2012 (137)
36 ILLUMINA ss481877443 May 04, 2012 (137)
37 ILLUMINA ss482834233 Sep 08, 2015 (146)
38 ILLUMINA ss485716827 May 04, 2012 (137)
39 ILLUMINA ss537577472 Sep 08, 2015 (146)
40 TISHKOFF ss558152862 Apr 25, 2013 (138)
41 SSMP ss651997780 Apr 25, 2013 (138)
42 ILLUMINA ss779004237 Sep 08, 2015 (146)
43 ILLUMINA ss783304060 Sep 08, 2015 (146)
44 ILLUMINA ss784256253 Sep 08, 2015 (146)
45 ILLUMINA ss825620339 Apr 01, 2015 (144)
46 ILLUMINA ss832565436 Sep 08, 2015 (146)
47 ILLUMINA ss833167186 Jul 13, 2019 (153)
48 ILLUMINA ss834466641 Sep 08, 2015 (146)
49 EVA-GONL ss981174023 Aug 21, 2014 (142)
50 JMKIDD_LAB ss1072331836 Aug 21, 2014 (142)
51 1000GENOMES ss1313634965 Aug 21, 2014 (142)
52 DDI ss1430220047 Apr 01, 2015 (144)
53 EVA_GENOME_DK ss1580979738 Apr 01, 2015 (144)
54 EVA_DECODE ss1590689096 Apr 01, 2015 (144)
55 EVA_UK10K_ALSPAC ss1612126565 Apr 01, 2015 (144)
56 EVA_UK10K_TWINSUK ss1655120598 Apr 01, 2015 (144)
57 EVA_SVP ss1712737580 Apr 01, 2015 (144)
58 ILLUMINA ss1752569210 Sep 08, 2015 (146)
59 HAMMER_LAB ss1802941874 Sep 08, 2015 (146)
60 WEILL_CORNELL_DGM ss1924431028 Feb 12, 2016 (147)
61 ILLUMINA ss1946136880 Feb 12, 2016 (147)
62 ILLUMINA ss1958760613 Feb 12, 2016 (147)
63 GENOMED ss1969993111 Jul 19, 2016 (147)
64 JJLAB ss2022808817 Sep 14, 2016 (149)
65 USC_VALOUEV ss2150959378 Dec 20, 2016 (150)
66 HUMAN_LONGEVITY ss2270823114 Dec 20, 2016 (150)
67 SYSTEMSBIOZJU ss2625902752 Nov 08, 2017 (151)
68 ILLUMINA ss2634235409 Nov 08, 2017 (151)
69 GRF ss2706481031 Nov 08, 2017 (151)
70 ILLUMINA ss2711028342 Nov 08, 2017 (151)
71 ILLUMINA ss2711028343 Nov 08, 2017 (151)
72 GNOMAD ss2820416330 Nov 08, 2017 (151)
73 AFFY ss2985314022 Nov 08, 2017 (151)
74 AFFY ss2985942268 Nov 08, 2017 (151)
75 SWEGEN ss2996329025 Nov 08, 2017 (151)
76 ILLUMINA ss3022459797 Nov 08, 2017 (151)
77 BIOINF_KMB_FNS_UNIBA ss3025187392 Nov 08, 2017 (151)
78 CSHL ss3346205835 Nov 08, 2017 (151)
79 ILLUMINA ss3625864631 Oct 12, 2018 (152)
80 ILLUMINA ss3629161455 Oct 12, 2018 (152)
81 ILLUMINA ss3632164706 Oct 12, 2018 (152)
82 ILLUMINA ss3633362616 Oct 12, 2018 (152)
83 ILLUMINA ss3634082705 Oct 12, 2018 (152)
84 ILLUMINA ss3634987851 Oct 12, 2018 (152)
85 ILLUMINA ss3635764997 Oct 12, 2018 (152)
86 ILLUMINA ss3636696627 Oct 12, 2018 (152)
87 ILLUMINA ss3637517594 Oct 12, 2018 (152)
88 ILLUMINA ss3638534343 Oct 12, 2018 (152)
89 ILLUMINA ss3639269590 Oct 12, 2018 (152)
90 ILLUMINA ss3639657502 Oct 12, 2018 (152)
91 ILLUMINA ss3640695144 Oct 12, 2018 (152)
92 ILLUMINA ss3643481818 Oct 12, 2018 (152)
93 ILLUMINA ss3644869750 Oct 12, 2018 (152)
94 ILLUMINA ss3652952182 Oct 12, 2018 (152)
95 ILLUMINA ss3654086657 Oct 12, 2018 (152)
96 EGCUT_WGS ss3664215749 Jul 13, 2019 (153)
97 EVA_DECODE ss3713970689 Jul 13, 2019 (153)
98 ILLUMINA ss3726207480 Jul 13, 2019 (153)
99 ACPOP ss3732025334 Jul 13, 2019 (153)
100 ILLUMINA ss3744247762 Jul 13, 2019 (153)
101 ILLUMINA ss3745288021 Jul 13, 2019 (153)
102 EVA ss3762977757 Jul 13, 2019 (153)
103 PAGE_CC ss3771181836 Jul 13, 2019 (153)
104 ILLUMINA ss3772782402 Jul 13, 2019 (153)
105 PACBIO ss3785001832 Jul 13, 2019 (153)
106 PACBIO ss3790422119 Jul 13, 2019 (153)
107 PACBIO ss3795298585 Jul 13, 2019 (153)
108 KHV_HUMAN_GENOMES ss3806146373 Jul 13, 2019 (153)
109 EVA ss3829056994 Apr 26, 2020 (154)
110 EVA ss3837988459 Apr 26, 2020 (154)
111 HGDP ss3847778687 Apr 26, 2020 (154)
112 SGDP_PRJ ss3861063726 Apr 26, 2020 (154)
113 KRGDB ss3907502617 Apr 26, 2020 (154)
114 KOGIC ss3955970449 Apr 26, 2020 (154)
115 EVA ss3984541714 Apr 26, 2021 (155)
116 EVA ss3985120071 Apr 26, 2021 (155)
117 EVA ss4017189176 Apr 26, 2021 (155)
118 TOPMED ss4647388593 Apr 26, 2021 (155)
119 TOMMO_GENOMICS ss5170085799 Apr 26, 2021 (155)
120 1000G_HIGH_COVERAGE ss5262640289 Oct 13, 2022 (156)
121 EVA ss5315025690 Oct 13, 2022 (156)
122 EVA ss5355214899 Oct 13, 2022 (156)
123 HUGCELL_USP ss5461007957 Oct 13, 2022 (156)
124 EVA ss5507892768 Oct 13, 2022 (156)
125 1000G_HIGH_COVERAGE ss5545570080 Oct 13, 2022 (156)
126 SANFORD_IMAGENETICS ss5624580019 Oct 13, 2022 (156)
127 SANFORD_IMAGENETICS ss5637044268 Oct 13, 2022 (156)
128 TOMMO_GENOMICS ss5705679167 Oct 13, 2022 (156)
129 EVA ss5799638802 Oct 13, 2022 (156)
130 YY_MCH ss5805959553 Oct 13, 2022 (156)
131 EVA ss5834422759 Oct 13, 2022 (156)
132 EVA ss5847259933 Oct 13, 2022 (156)
133 EVA ss5848038924 Oct 13, 2022 (156)
134 EVA ss5854649146 Oct 13, 2022 (156)
135 EVA ss5892716824 Oct 13, 2022 (156)
136 EVA ss5965451048 Oct 13, 2022 (156)
137 EVA ss5979728988 Oct 13, 2022 (156)
138 1000Genomes NC_000005.9 - 2279866 Oct 12, 2018 (152)
139 1000Genomes_30x NC_000005.10 - 2279752 Oct 13, 2022 (156)
140 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 2279866 Oct 12, 2018 (152)
141 Genetic variation in the Estonian population NC_000005.9 - 2279866 Oct 12, 2018 (152)
142 The Danish reference pan genome NC_000005.9 - 2279866 Apr 26, 2020 (154)
143 gnomAD - Genomes NC_000005.10 - 2279752 Apr 26, 2021 (155)
144 Genome of the Netherlands Release 5 NC_000005.9 - 2279866 Apr 26, 2020 (154)
145 HGDP-CEPH-db Supplement 1 NC_000005.8 - 2332866 Apr 26, 2020 (154)
146 HapMap NC_000005.10 - 2279752 Apr 26, 2020 (154)
147 KOREAN population from KRGDB NC_000005.9 - 2279866 Apr 26, 2020 (154)
148 Korean Genome Project NC_000005.10 - 2279752 Apr 26, 2020 (154)
149 Northern Sweden NC_000005.9 - 2279866 Jul 13, 2019 (153)
150 The PAGE Study NC_000005.10 - 2279752 Jul 13, 2019 (153)
151 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 2279866 Apr 26, 2021 (155)
152 CNV burdens in cranial meningiomas NC_000005.9 - 2279866 Apr 26, 2021 (155)
153 Qatari NC_000005.9 - 2279866 Apr 26, 2020 (154)
154 SGDP_PRJ NC_000005.9 - 2279866 Apr 26, 2020 (154)
155 Siberian NC_000005.9 - 2279866 Apr 26, 2020 (154)
156 8.3KJPN NC_000005.9 - 2279866 Apr 26, 2021 (155)
157 14KJPN NC_000005.10 - 2279752 Oct 13, 2022 (156)
158 TopMed NC_000005.10 - 2279752 Apr 26, 2021 (155)
159 UK 10K study - Twins NC_000005.9 - 2279866 Oct 12, 2018 (152)
160 A Vietnamese Genetic Variation Database NC_000005.9 - 2279866 Jul 13, 2019 (153)
161 ALFA NC_000005.10 - 2279752 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)
rs58172195 May 24, 2008 (130)
rs386621046 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
456579, ss84968100, ss111307023, ss161950680, ss164049333, ss199779596, ss206889617, ss253159583, ss278137033, ss481844744, ss825620339, ss1590689096, ss1712737580, ss3639269590, ss3639657502, ss3643481818, ss3847778687 NC_000005.8:2332865:G:A NC_000005.10:2279751:G:A (self)
25180557, 14003747, 9953997, 7144677, 6216926, 14680011, 5310199, 345998, 91078, 6472958, 13080706, 3475732, 28055106, 14003747, 3105010, ss221472332, ss232796483, ss240000247, ss481877443, ss482834233, ss485716827, ss537577472, ss558152862, ss651997780, ss779004237, ss783304060, ss784256253, ss832565436, ss833167186, ss834466641, ss981174023, ss1072331836, ss1313634965, ss1430220047, ss1580979738, ss1612126565, ss1655120598, ss1752569210, ss1802941874, ss1924431028, ss1946136880, ss1958760613, ss1969993111, ss2022808817, ss2150959378, ss2625902752, ss2634235409, ss2706481031, ss2711028342, ss2711028343, ss2820416330, ss2985314022, ss2985942268, ss2996329025, ss3022459797, ss3346205835, ss3625864631, ss3629161455, ss3632164706, ss3633362616, ss3634082705, ss3634987851, ss3635764997, ss3636696627, ss3637517594, ss3638534343, ss3640695144, ss3644869750, ss3652952182, ss3654086657, ss3664215749, ss3732025334, ss3744247762, ss3745288021, ss3762977757, ss3772782402, ss3785001832, ss3790422119, ss3795298585, ss3829056994, ss3837988459, ss3861063726, ss3907502617, ss3984541714, ss3985120071, ss4017189176, ss5170085799, ss5315025690, ss5355214899, ss5507892768, ss5624580019, ss5637044268, ss5799638802, ss5834422759, ss5847259933, ss5848038924, ss5965451048, ss5979728988 NC_000005.9:2279865:G:A NC_000005.10:2279751:G:A (self)
33096015, 178063467, 2791730, 12348450, 403305, 39516271, 484766150, 3414610485, ss2270823114, ss3025187392, ss3713970689, ss3726207480, ss3771181836, ss3806146373, ss3955970449, ss4647388593, ss5262640289, ss5461007957, ss5545570080, ss5705679167, ss5805959553, ss5854649146, ss5892716824 NC_000005.10:2279751:G:A NC_000005.10:2279751:G:A (self)
ss1359993, ss3672021, ss23742133, ss44605132, ss65720884, ss66854269, ss67895932, ss68030337, ss68924209, ss71594987, ss75870784, ss79289821, ss83613599, ss98237388, ss105900504, ss120243078, ss122952702, ss154481982, ss159656392, ss160968501, ss172433781, ss174786352, ss244256903 NT_006576.16:2269865:G:A NC_000005.10:2279751:G:A (self)
Help

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

No publications for rs923048

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