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rs104894095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894095(C;C)
Make rs104894095(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971200
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs104894095
ebirs104894095
HLIrs104894095
Exacrs104894095
Varsomers104894095
Maprs104894095
PheGenIrs104894095
hapmaprs104894095
1000 genomesrs104894095
hgdprs104894095
ensemblrs104894095
gopubmedrs104894095
geneviewrs104894095
scholarrs104894095
googlers104894095
pharmgkbrs104894095
gwascentralrs104894095
openSNPrs104894095
23andMers104894095
23andMe allrs104894095
SNP Nexus

SNPshotrs104894095
SNPdbers104894095
MSV3drs104894095
GWAS Ctlgrs104894095
Max Magnitude0
OMIM600160
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104894095(A,C;A,C)
Alt rs104894095(A,C;A,C)
Reference rs104894095(G;G)
Significance Other
Disease Melanoma Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided
Reversed 1
HGVS NC_000009.11:g.21971199C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010021.2, RCV000160421.3, RCV000205342.1, RCV000212399.1,