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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
dbSNP (classic)rs104894109
ClinGenrs104894109
ebirs104894109
HLIrs104894109
Exacrs104894109
Gnomadrs104894109
Varsomers104894109
LitVarrs104894109
Maprs104894109
PheGenIrs104894109
Biobankrs104894109
1000 genomesrs104894109
hgdprs104894109
ensemblrs104894109
geneviewrs104894109
scholarrs104894109
googlers104894109
pharmgkbrs104894109
gwascentralrs104894109
openSNPrs104894109
23andMers104894109
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 Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21971191C>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000010032.2, RCV000471463.1,