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rs10964862

From SNPedia

Orientationplus
Stabilizedplus
Make rs10964862(A;A)
Make rs10964862(A;C)
Make rs10964862(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position21151554
is asnp
is mentioned by
dbSNPrs10964862
ebirs10964862
HLIrs10964862
Exacrs10964862
Varsomers10964862
Maprs10964862
PheGenIrs10964862
hapmaprs10964862
1000 genomesrs10964862
hgdprs10964862
ensemblrs10964862
gopubmedrs10964862
geneviewrs10964862
scholarrs10964862
googlers10964862
pharmgkbrs10964862
gwascentralrs10964862
openSNPrs10964862
23andMers10964862
23andMe allrs10964862
SNP Nexus

SNPshotrs10964862
SNPdbers10964862
MSV3drs10964862
GWAS Ctlgrs10964862
GMAF0.2998
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 20574843OA-icon.png] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations


[PMID 23209811OA-icon.png] Influence of genetic variants in type I interferon genes on melanoma survival and therapy