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rs104894098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs104894098(A;A)
Make rs104894098(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position21970982
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs104894098
ebirs104894098
HLIrs104894098
Exacrs104894098
Varsomers104894098
Maprs104894098
PheGenIrs104894098
hapmaprs104894098
1000 genomesrs104894098
hgdprs104894098
ensemblrs104894098
gopubmedrs104894098
geneviewrs104894098
scholarrs104894098
googlers104894098
pharmgkbrs104894098
gwascentralrs104894098
openSNPrs104894098
23andMers104894098
23andMe allrs104894098
SNP Nexus

SNPshotrs104894098
SNPdbers104894098
MSV3drs104894098
GWAS Ctlgrs104894098
Max Magnitude0
OMIM600160
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104894098(A;A)
Alt rs104894098(A;A)
Reference rs104894098(T;T)
Significance Other
Disease Melanoma Hereditary cancer-predisposing syndrome not provided Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cancer-predisposing syndrome not provided Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21970981A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010027.2, RCV000160413.4, RCV000212403.1, RCV000227154.1,