rs10964862
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10964862(A;A) |
Make rs10964862(A;C) |
Make rs10964862(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 21151554 |
is a | snp |
is | mentioned by |
dbSNP | rs10964862 |
dbSNP (classic) | rs10964862 |
ClinGen | rs10964862 |
ebi | rs10964862 |
HLI | rs10964862 |
Exac | rs10964862 |
Gnomad | rs10964862 |
Varsome | rs10964862 |
LitVar | rs10964862 |
Map | rs10964862 |
PheGenI | rs10964862 |
Biobank | rs10964862 |
1000 genomes | rs10964862 |
hgdp | rs10964862 |
ensembl | rs10964862 |
geneview | rs10964862 |
scholar | rs10964862 |
rs10964862 | |
pharmgkb | rs10964862 |
gwascentral | rs10964862 |
openSNP | rs10964862 |
23andMe | rs10964862 |
SNPshot | rs10964862 |
SNPdbe | rs10964862 |
MSV3d | rs10964862 |
GWAS Ctlg | rs10964862 |
GMAF | 0.2998 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
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[PMID 20574843] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
[PMID 23209811] Influence of genetic variants in type I interferon genes on melanoma survival and therapy