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rs121913394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913394(A;A)
Make rs121913394(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224549
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913394
dbSNP (old)rs121913394
ClinGenrs121913394
ebirs121913394
HLIrs121913394
Exacrs121913394
Gnomadrs121913394
Varsomers121913394
Maprs121913394
PheGenIrs121913394
Biobankrs121913394
1000 genomesrs121913394
hgdprs121913394
ensemblrs121913394
gopubmedrs121913394
geneviewrs121913394
scholarrs121913394
googlers121913394
pharmgkbrs121913394
gwascentralrs121913394
openSNPrs121913394
23andMers121913394
23andMe allrs121913394
SNPshotrs121913394
SNPdbers121913394
MSV3drs121913394
GWAS Ctlgrs121913394
Max Magnitude0
ClinVar
Risk rs121913394(A;A)
Alt rs121913394(A;A)
Reference Rs121913394(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene CTNNB1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000003.11:g.41266040G>A
CLNSRC
CLNACC RCV000419765.1,