Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104894109(G;T)
Make rs104894109(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971192
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs104894109
ebirs104894109
HLIrs104894109
Exacrs104894109
Varsomers104894109
Maprs104894109
PheGenIrs104894109
hapmaprs104894109
1000 genomesrs104894109
hgdprs104894109
ensemblrs104894109
gopubmedrs104894109
geneviewrs104894109
scholarrs104894109
googlers104894109
pharmgkbrs104894109
gwascentralrs104894109
openSNPrs104894109
23andMers104894109
23andMe allrs104894109
SNP Nexus

SNPshotrs104894109
SNPdbers104894109
MSV3drs104894109
GWAS Ctlgrs104894109
Max Magnitude0
OMIM600160
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104894109(T;T)
Alt rs104894109(T;T)
Reference rs104894109(G;G)
Significance Other
Disease Melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2
Reversed 1
HGVS NC_000009.11:g.21971191C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010032.2,