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rs104894099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs104894099(G;G)
Make rs104894099(G;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971183
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs104894099
ebirs104894099
HLIrs104894099
Exacrs104894099
Varsomers104894099
Maprs104894099
PheGenIrs104894099
hapmaprs104894099
1000 genomesrs104894099
hgdprs104894099
ensemblrs104894099
gopubmedrs104894099
geneviewrs104894099
scholarrs104894099
googlers104894099
pharmgkbrs104894099
gwascentralrs104894099
openSNPrs104894099
23andMers104894099
23andMe allrs104894099
SNP Nexus

SNPshotrs104894099
SNPdbers104894099
MSV3drs104894099
GWAS Ctlgrs104894099
Max Magnitude0
OMIM600160
Desc
Variant0016
Relatedalso
ClinVar
Risk rs104894099(G;G)
Alt rs104894099(G;G)
Reference rs104894099(T;T)
Significance Other
Disease Melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2
Reversed 1
HGVS NC_000009.11:g.21971182A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010030.2,