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rs121913386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913386(C;T)
Make rs121913386(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971018
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs121913386
dbSNP (old)rs121913386
ClinGenrs121913386
ebirs121913386
HLIrs121913386
Exacrs121913386
Gnomadrs121913386
Varsomers121913386
Maprs121913386
PheGenIrs121913386
Biobankrs121913386
1000 genomesrs121913386
hgdprs121913386
ensemblrs121913386
gopubmedrs121913386
geneviewrs121913386
scholarrs121913386
googlers121913386
pharmgkbrs121913386
gwascentralrs121913386
openSNPrs121913386
23andMers121913386
23andMe allrs121913386
SNPshotrs121913386
SNPdbers121913386
MSV3drs121913386
GWAS Ctlgrs121913386
Max Magnitude0
ClinVar
Risk rs121913386(A;A) rs121913386(T;T)
Alt rs121913386(A;A) rs121913386(T;T)
Reference Rs121913386(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma Malignant melanoma of skin Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Variation info
Gene CDKN2A
CLNDBN Malignant melanoma Malignant melanoma of skin Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck
Reversed 1
HGVS NC_000009.11:g.21971017G>A; NC_000009.11:g.21971017G>T
CLNSRC
CLNACC RCV000424989.1, RCV000425751.1, RCV000435136.1, RCV000442671.1, RCV000444494.1, RCV000420475.1, RCV000429868.1, RCV000438111.1, RCV000440098.1,