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rs7855483

From SNPedia

Orientationplus
Stabilizedplus
Make rs7855483(C;C)
Make rs7855483(C;T)
Make rs7855483(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position32372464
is asnp
is mentioned by
dbSNPrs7855483
ebirs7855483
HLIrs7855483
Exacrs7855483
Varsomers7855483
Maprs7855483
PheGenIrs7855483
hapmaprs7855483
1000 genomesrs7855483
hgdprs7855483
ensemblrs7855483
gopubmedrs7855483
geneviewrs7855483
scholarrs7855483
googlers7855483
pharmgkbrs7855483
gwascentralrs7855483
openSNPrs7855483
23andMers7855483
23andMe allrs7855483
SNP Nexus

SNPshotrs7855483
SNPdbers7855483
MSV3drs7855483
GWAS Ctlgrs7855483
GMAF0.2406
Max Magnitude
? (C;C) (C;T) (T;T) 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