Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs2491231

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr13:28036046 (GRCh38.p13) 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>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.403162 (106713/264690, TOPMED)
A=0.290256 (72669/250362, GnomAD_exome)
A=0.389470 (54497/139926, GnomAD) (+ 22 more)
A=0.277337 (37263/134360, ALFA)
A=0.300683 (36453/121234, ExAC)
A=0.35788 (5998/16760, 8.3KJPN)
A=0.38359 (4989/13006, GO-ESP)
A=0.4367 (2187/5008, 1000G)
A=0.2623 (1175/4480, Estonian)
A=0.2086 (804/3854, ALSPAC)
A=0.2195 (814/3708, TWINSUK)
A=0.2836 (831/2930, KOREAN)
A=0.3762 (784/2084, HGDP_Stanford)
A=0.4968 (939/1890, HapMap)
A=0.2686 (492/1832, Korea1K)
A=0.225 (225/998, GoNL)
A=0.301 (185/614, Vietnamese)
A=0.182 (109/600, NorthernSweden)
A=0.257 (137/534, MGP)
A=0.239 (106/444, SGDP_PRJ)
A=0.178 (54/304, FINRISK)
A=0.389 (84/216, Qatari)
A=0.35 (22/62, Ancient Sardinia)
A=0.13 (7/54, Siberian)
A=0.25 (10/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FLT3 : Intron Variant
Publications
1 citation
Genomic View
See rs on genome
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.p13 chr 13 NC_000013.11:g.28036046A>G
GRCh37.p13 chr 13 NC_000013.10:g.28610183A>G
FLT3 RefSeqGene (LRG_457) NG_007066.1:g.69523T>C
Gene: FLT3, fms related receptor tyrosine kinase 3 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
FLT3 transcript variant 1 NM_004119.3:c.1310-3T>C N/A Intron Variant
FLT3 transcript variant 2 NR_130706.2:n. N/A Intron Variant
FLT3 transcript variant X1 XM_011535015.2:c.1253-3T>C N/A Intron Variant
FLT3 transcript variant X4 XM_011535017.2:c.785-3T>C N/A Intron Variant
FLT3 transcript variant X5 XM_011535018.2:c.785-3T>C N/A Intron Variant
FLT3 transcript variant X2 XM_017020486.1:c.1094-3T>C N/A Intron Variant
FLT3 transcript variant X3 XM_017020487.1:c.785-3T>C N/A Intron Variant
FLT3 transcript variant X6 XM_017020488.1:c.431-3T>C N/A Intron Variant
FLT3 transcript variant X7 XM_017020489.1:c.413-3T>C 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

ALFA Allele Frequency (New)
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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 134360 A=0.277337 G=0.722663
European Sub 101924 A=0.228945 G=0.771055
African Sub 9786 A=0.7065 G=0.2935
African Others Sub 328 A=0.790 G=0.210
African American Sub 9458 A=0.7036 G=0.2964
Asian Sub 580 A=0.260 G=0.740
East Asian Sub 468 A=0.284 G=0.716
Other Asian Sub 112 A=0.161 G=0.839
Latin American 1 Sub 1036 A=0.4237 G=0.5763
Latin American 2 Sub 5556 A=0.2860 G=0.7140
South Asian Sub 5018 A=0.4004 G=0.5996
Other Sub 10460 A=0.27017 G=0.72983


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 A=0.403162 G=0.596838
gnomAD - Exomes Global Study-wide 250362 A=0.290256 G=0.709744
gnomAD - Exomes European Sub 134376 A=0.221810 G=0.778190
gnomAD - Exomes Asian Sub 48988 A=0.34237 G=0.65763
gnomAD - Exomes American Sub 34580 A=0.28222 G=0.71778
gnomAD - Exomes African Sub 16222 A=0.73178 G=0.26822
gnomAD - Exomes Ashkenazi Jewish Sub 10066 A=0.27836 G=0.72164
gnomAD - Exomes Other Sub 6130 A=0.2706 G=0.7294
gnomAD - Genomes Global Study-wide 139926 A=0.389470 G=0.610530
gnomAD - Genomes European Sub 75840 A=0.22533 G=0.77467
gnomAD - Genomes African Sub 41906 A=0.72238 G=0.27762
gnomAD - Genomes American Sub 13594 A=0.33809 G=0.66191
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=0.2769 G=0.7231
gnomAD - Genomes East Asian Sub 3120 A=0.2548 G=0.7452
gnomAD - Genomes Other Sub 2144 A=0.3848 G=0.6152
ExAC Global Study-wide 121234 A=0.300683 G=0.699317
ExAC Europe Sub 73294 A=0.22718 G=0.77282
ExAC Asian Sub 25136 A=0.34982 G=0.65018
ExAC American Sub 11566 A=0.28143 G=0.71857
ExAC African Sub 10332 A=0.72435 G=0.27565
ExAC Other Sub 906 A=0.298 G=0.702
8.3KJPN JAPANESE Study-wide 16760 A=0.35788 G=0.64212
GO Exome Sequencing Project Global Study-wide 13006 A=0.38359 G=0.61641
GO Exome Sequencing Project European American Sub 8600 A=0.2179 G=0.7821
GO Exome Sequencing Project African American Sub 4406 A=0.7070 G=0.2930
1000Genomes Global Study-wide 5008 A=0.4367 G=0.5633
1000Genomes African Sub 1322 A=0.8056 G=0.1944
1000Genomes East Asian Sub 1008 A=0.2649 G=0.7351
1000Genomes Europe Sub 1006 A=0.2276 G=0.7724
1000Genomes South Asian Sub 978 A=0.439 G=0.561
1000Genomes American Sub 694 A=0.284 G=0.716
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.2623 G=0.7377
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.2086 G=0.7914
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.2195 G=0.7805
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.2836 G=0.7164
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.3762 G=0.6238
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.283 G=0.717
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.401 G=0.599
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.366 G=0.634
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.228 G=0.772
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.843 G=0.157
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.273 G=0.727
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.29 G=0.71
HapMap Global Study-wide 1890 A=0.4968 G=0.5032
HapMap American Sub 768 A=0.346 G=0.654
HapMap African Sub 692 A=0.790 G=0.210
HapMap Asian Sub 254 A=0.303 G=0.697
HapMap Europe Sub 176 A=0.278 G=0.722
Korean Genome Project KOREAN Study-wide 1832 A=0.2686 G=0.7314
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.225 G=0.775
A Vietnamese Genetic Variation Database Global Study-wide 614 A=0.301 G=0.699
Northern Sweden ACPOP Study-wide 600 A=0.182 G=0.818
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 A=0.257 G=0.743
SGDP_PRJ Global Study-wide 444 A=0.239 G=0.761
FINRISK Finnish from FINRISK project Study-wide 304 A=0.178 G=0.822
Qatari Global Study-wide 216 A=0.389 G=0.611
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 62 A=0.35 G=0.65
Siberian Global Study-wide 54 A=0.13 G=0.87
The Danish reference pan genome Danish Study-wide 40 A=0.25 G=0.75
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 A= G
GRCh38.p13 chr 13 NC_000013.11:g.28036046= NC_000013.11:g.28036046A>G
GRCh37.p13 chr 13 NC_000013.10:g.28610183= NC_000013.10:g.28610183A>G
FLT3 RefSeqGene (LRG_457) NG_007066.1:g.69523= NG_007066.1:g.69523T>C
FLT3 transcript variant 1 NM_004119.2:c.1310-3= NM_004119.2:c.1310-3T>C
FLT3 transcript variant 1 NM_004119.3:c.1310-3= NM_004119.3:c.1310-3T>C
FLT3 transcript variant X1 XM_005266318.1:c.1310-3= XM_005266318.1:c.1310-3T>C
FLT3 transcript variant X2 XM_005266319.1:c.1310-3= XM_005266319.1:c.1310-3T>C
FLT3 transcript variant X1 XM_011535015.2:c.1253-3= XM_011535015.2:c.1253-3T>C
FLT3 transcript variant X4 XM_011535017.2:c.785-3= XM_011535017.2:c.785-3T>C
FLT3 transcript variant X5 XM_011535018.2:c.785-3= XM_011535018.2:c.785-3T>C
FLT3 transcript variant X2 XM_017020486.1:c.1094-3= XM_017020486.1:c.1094-3T>C
FLT3 transcript variant X3 XM_017020487.1:c.785-3= XM_017020487.1:c.785-3T>C
FLT3 transcript variant X6 XM_017020488.1:c.431-3= XM_017020488.1:c.431-3T>C
FLT3 transcript variant X7 XM_017020489.1:c.413-3= XM_017020489.1:c.413-3T>C
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#.

120 SubSNP, 25 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss3495514 Sep 28, 2001 (100)
2 SC_SNP ss13161596 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss16607931 Feb 27, 2004 (120)
4 CSHL-HAPMAP ss19264612 Feb 27, 2004 (120)
5 SSAHASNP ss21124639 Apr 05, 2004 (121)
6 PERLEGEN ss23967789 Sep 20, 2004 (123)
7 ABI ss40323144 Mar 14, 2006 (126)
8 ILLUMINA ss67257414 Nov 30, 2006 (127)
9 ILLUMINA ss67655977 Nov 30, 2006 (127)
10 ILLUMINA ss68206135 Dec 12, 2006 (127)
11 ILLUMINA ss70735772 May 26, 2008 (130)
12 ILLUMINA ss71305902 May 17, 2007 (127)
13 CANCER-GENOME ss74802661 Dec 07, 2007 (129)
14 ILLUMINA ss75508750 Dec 07, 2007 (129)
15 HGSV ss78227125 Dec 07, 2007 (129)
16 HGSV ss78848570 Dec 07, 2007 (129)
17 HGSV ss82680955 Dec 15, 2007 (130)
18 KRIBB_YJKIM ss84053649 Dec 15, 2007 (130)
19 HUMANGENOME_JCVI ss96954342 Feb 06, 2009 (130)
20 BGI ss103106215 Dec 01, 2009 (131)
21 1000GENOMES ss112644101 Jan 25, 2009 (130)
22 ILLUMINA-UK ss118400276 Feb 14, 2009 (130)
23 ENSEMBL ss137275184 Dec 01, 2009 (131)
24 ILLUMINA ss153915796 Dec 01, 2009 (131)
25 GMI ss154578077 Dec 01, 2009 (131)
26 ILLUMINA ss159393584 Dec 01, 2009 (131)
27 ILLUMINA ss160552472 Dec 01, 2009 (131)
28 COMPLETE_GENOMICS ss167782378 Jul 04, 2010 (132)
29 COMPLETE_GENOMICS ss170926239 Jul 04, 2010 (132)
30 ILLUMINA ss173369132 Jul 04, 2010 (132)
31 BCM-HGSC-SUB ss208588629 Jul 04, 2010 (132)
32 1000GENOMES ss211379380 Jul 14, 2010 (132)
33 1000GENOMES ss226096899 Jul 14, 2010 (132)
34 1000GENOMES ss236188898 Jul 15, 2010 (132)
35 1000GENOMES ss242696890 Jul 15, 2010 (132)
36 BL ss254882191 May 09, 2011 (134)
37 GMI ss281651543 May 04, 2012 (137)
38 GMI ss286674477 Apr 25, 2013 (138)
39 PJP ss291563989 May 09, 2011 (134)
40 ILLUMINA ss481424188 Sep 08, 2015 (146)
41 1000GENOMES ss491057559 May 04, 2012 (137)
42 CLINSEQ_SNP ss491677783 May 04, 2012 (137)
43 ILLUMINA ss536379922 Sep 08, 2015 (146)
44 TISHKOFF ss563568953 Apr 25, 2013 (138)
45 SSMP ss659164688 Apr 25, 2013 (138)
46 NHLBI-ESP ss713144132 Apr 25, 2013 (138)
47 ILLUMINA ss832905325 Jul 13, 2019 (153)
48 JMKIDD_LAB ss974486356 Aug 21, 2014 (142)
49 EVA-GONL ss990224105 Aug 21, 2014 (142)
50 JMKIDD_LAB ss1067540484 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1078960319 Aug 21, 2014 (142)
52 1000GENOMES ss1347603151 Aug 21, 2014 (142)
53 DDI ss1427139142 Apr 01, 2015 (144)
54 EVA_GENOME_DK ss1576692219 Apr 01, 2015 (144)
55 EVA_FINRISK ss1584086324 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1629948338 Apr 01, 2015 (144)
57 EVA_DECODE ss1642328799 Apr 01, 2015 (144)
58 EVA_UK10K_TWINSUK ss1672942371 Apr 01, 2015 (144)
59 EVA_EXAC ss1691239558 Apr 01, 2015 (144)
60 EVA_MGP ss1711353513 Apr 01, 2015 (144)
61 EVA_SVP ss1713378097 Apr 01, 2015 (144)
62 HAMMER_LAB ss1807539712 Sep 08, 2015 (146)
63 WEILL_CORNELL_DGM ss1933592887 Feb 12, 2016 (147)
64 GENOMED ss1966658543 Feb 12, 2016 (147)
65 JJLAB ss2027552115 Sep 14, 2016 (149)
66 USC_VALOUEV ss2155916643 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2195068095 Dec 20, 2016 (150)
68 TOPMED ss2359168413 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2628264201 Nov 08, 2017 (151)
70 ILLUMINA ss2635043626 Nov 08, 2017 (151)
71 GRF ss2700288796 Nov 08, 2017 (151)
72 GNOMAD ss2740336010 Nov 08, 2017 (151)
73 GNOMAD ss2749024424 Nov 08, 2017 (151)
74 GNOMAD ss2917897112 Nov 08, 2017 (151)
75 SWEGEN ss3010767688 Nov 08, 2017 (151)
76 BIOINF_KMB_FNS_UNIBA ss3027591505 Nov 08, 2017 (151)
77 TOPMED ss3188674392 Nov 08, 2017 (151)
78 CSHL ss3350380021 Nov 08, 2017 (151)
79 ILLUMINA ss3627028697 Oct 12, 2018 (152)
80 ILLUMINA ss3636223742 Oct 12, 2018 (152)
81 ILLUMINA ss3638001931 Oct 12, 2018 (152)
82 ILLUMINA ss3639013906 Oct 12, 2018 (152)
83 ILLUMINA ss3639817006 Oct 12, 2018 (152)
84 ILLUMINA ss3641039498 Oct 12, 2018 (152)
85 ILLUMINA ss3641334375 Oct 12, 2018 (152)
86 ILLUMINA ss3642992500 Oct 12, 2018 (152)
87 ILLUMINA ss3643868104 Oct 12, 2018 (152)
88 OMUKHERJEE_ADBS ss3646452093 Oct 12, 2018 (152)
89 URBANLAB ss3649995488 Oct 12, 2018 (152)
90 EGCUT_WGS ss3678028354 Jul 13, 2019 (153)
91 EVA_DECODE ss3694983449 Jul 13, 2019 (153)
92 ACPOP ss3739608718 Jul 13, 2019 (153)
93 EVA ss3751270851 Jul 13, 2019 (153)
94 PACBIO ss3787413116 Jul 13, 2019 (153)
95 PACBIO ss3792486013 Jul 13, 2019 (153)
96 PACBIO ss3797369732 Jul 13, 2019 (153)
97 KHV_HUMAN_GENOMES ss3816601655 Jul 13, 2019 (153)
98 EVA ss3824799152 Apr 27, 2020 (154)
99 EVA ss3825834613 Apr 27, 2020 (154)
100 EVA ss3833464659 Apr 27, 2020 (154)
101 EVA ss3840309468 Apr 27, 2020 (154)
102 EVA ss3845794169 Apr 27, 2020 (154)
103 HGDP ss3847472993 Apr 27, 2020 (154)
104 SGDP_PRJ ss3879651981 Apr 27, 2020 (154)
105 KRGDB ss3928472465 Apr 27, 2020 (154)
106 KOGIC ss3973259805 Apr 27, 2020 (154)
107 FSA-LAB ss3984044392 Apr 26, 2021 (155)
108 EVA ss3985630656 Apr 26, 2021 (155)
109 EVA ss3986062266 Apr 26, 2021 (155)
110 EVA ss3986597806 Apr 26, 2021 (155)
111 EVA ss4017624235 Apr 26, 2021 (155)
112 TOPMED ss4940853787 Apr 26, 2021 (155)
113 TOMMO_GENOMICS ss5209297994 Apr 26, 2021 (155)
114 CPQ_GEN_INCA ss5236853865 Apr 26, 2021 (155)
115 CPQ_GEN_INCA ss5236856900 Apr 26, 2021 (155)
116 CPQ_GEN_INCA ss5236856901 Apr 26, 2021 (155)
117 CPQ_GEN_INCA ss5236856902 Apr 26, 2021 (155)
118 CPQ_GEN_INCA ss5236856903 Apr 26, 2021 (155)
119 CPQ_GEN_INCA ss5236856904 Apr 26, 2021 (155)
120 EVA ss5237223486 Apr 26, 2021 (155)
121 1000Genomes NC_000013.10 - 28610183 Oct 12, 2018 (152)
122 The Avon Longitudinal Study of Parents and Children NC_000013.10 - 28610183 Oct 12, 2018 (152)
123 Genetic variation in the Estonian population NC_000013.10 - 28610183 Oct 12, 2018 (152)
124 ExAC NC_000013.10 - 28610183 Oct 12, 2018 (152)
125 FINRISK NC_000013.10 - 28610183 Apr 27, 2020 (154)
126 The Danish reference pan genome NC_000013.10 - 28610183 Apr 27, 2020 (154)
127 gnomAD - Genomes NC_000013.11 - 28036046 Apr 26, 2021 (155)
128 gnomAD - Exomes NC_000013.10 - 28610183 Jul 13, 2019 (153)
129 GO Exome Sequencing Project NC_000013.10 - 28610183 Oct 12, 2018 (152)
130 Genome of the Netherlands Release 5 NC_000013.10 - 28610183 Apr 27, 2020 (154)
131 HGDP-CEPH-db Supplement 1 NC_000013.9 - 27508183 Apr 27, 2020 (154)
132 HapMap NC_000013.11 - 28036046 Apr 27, 2020 (154)
133 KOREAN population from KRGDB NC_000013.10 - 28610183 Apr 27, 2020 (154)
134 Korean Genome Project NC_000013.11 - 28036046 Apr 27, 2020 (154)
135 Medical Genome Project healthy controls from Spanish population NC_000013.10 - 28610183 Apr 27, 2020 (154)
136 Northern Sweden NC_000013.10 - 28610183 Jul 13, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000013.10 - 28610183 Apr 26, 2021 (155)
138 Qatari NC_000013.10 - 28610183 Apr 27, 2020 (154)
139 SGDP_PRJ NC_000013.10 - 28610183 Apr 27, 2020 (154)
140 Siberian NC_000013.10 - 28610183 Apr 27, 2020 (154)
141 8.3KJPN NC_000013.10 - 28610183 Apr 26, 2021 (155)
142 TopMed NC_000013.11 - 28036046 Apr 26, 2021 (155)
143 UK 10K study - Twins NC_000013.10 - 28610183 Oct 12, 2018 (152)
144 A Vietnamese Genetic Variation Database NC_000013.10 - 28610183 Jul 13, 2019 (153)
145 ALFA NC_000013.11 - 28036046 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)
rs60899063 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
150885, ss78227125, ss78848570, ss82680955, ss112644101, ss118400276, ss167782378, ss170926239, ss208588629, ss211379380, ss254882191, ss281651543, ss286674477, ss291563989, ss491677783, ss1642328799, ss1713378097, ss2635043626, ss3639013906, ss3639817006, ss3642992500, ss3643868104, ss3847472993 NC_000013.9:27508182:A:G NC_000013.11:28036045:A:G (self)
60450878, 33574152, 23766602, 1564311, 82785, 3232585, 9577975, 1256540, 14980730, 35649859, 469273, 12893583, 856583, 15634817, 31668961, 8432997, 67267301, 33574152, 7447562, ss226096899, ss236188898, ss242696890, ss481424188, ss491057559, ss536379922, ss563568953, ss659164688, ss713144132, ss832905325, ss974486356, ss990224105, ss1067540484, ss1078960319, ss1347603151, ss1427139142, ss1576692219, ss1584086324, ss1629948338, ss1672942371, ss1691239558, ss1711353513, ss1807539712, ss1933592887, ss1966658543, ss2027552115, ss2155916643, ss2359168413, ss2628264201, ss2700288796, ss2740336010, ss2749024424, ss2917897112, ss3010767688, ss3350380021, ss3627028697, ss3636223742, ss3638001931, ss3641039498, ss3641334375, ss3646452093, ss3678028354, ss3739608718, ss3751270851, ss3787413116, ss3792486013, ss3797369732, ss3824799152, ss3825834613, ss3833464659, ss3840309468, ss3879651981, ss3928472465, ss3984044392, ss3985630656, ss3986062266, ss3986597806, ss4017624235, ss5209297994, ss5236853865, ss5236856900, ss5236856901, ss5236856902, ss5236856903, ss5236856904 NC_000013.10:28610182:A:G NC_000013.11:28036045:A:G (self)
426263473, 954272, 29637806, 97801116, 156399445, 5073367143, ss2195068095, ss3027591505, ss3188674392, ss3649995488, ss3694983449, ss3816601655, ss3845794169, ss3973259805, ss4940853787, ss5237223486 NC_000013.11:28036045:A:G NC_000013.11:28036045:A:G (self)
ss13161596 NT_009799.12:9590182:A:G NC_000013.11:28036045:A:G (self)
ss16607931, ss19264612, ss21124639 NT_024524.13:9590182:A:G NC_000013.11:28036045:A:G (self)
ss3495514, ss23967789, ss40323144, ss67257414, ss67655977, ss68206135, ss70735772, ss71305902, ss74802661, ss75508750, ss84053649, ss96954342, ss103106215, ss137275184, ss153915796, ss154578077, ss159393584, ss160552472, ss173369132 NT_024524.14:9590182:A:G NC_000013.11:28036045:A:G (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 rs2491231
PMID Title Author Year Journal
30867801 Genetic alterations of triple negative breast cancer (TNBC) in women from Northeastern Mexico. Uscanga-Perales GI et al. 2019 Oncology letters
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.post596+ae089ad