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rs121913395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913395(A;A)
Make rs121913395(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224573
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913395
dbSNP (old)rs121913395
ClinGenrs121913395
ebirs121913395
HLIrs121913395
Exacrs121913395
Gnomadrs121913395
Varsomers121913395
LitVarrs121913395
Maprs121913395
PheGenIrs121913395
Biobankrs121913395
1000 genomesrs121913395
hgdprs121913395
ensemblrs121913395
gopubmedrs121913395
geneviewrs121913395
scholarrs121913395
googlers121913395
pharmgkbrs121913395
gwascentralrs121913395
openSNPrs121913395
23andMers121913395
23andMe allrs121913395
SNPshotrs121913395
SNPdbers121913395
MSV3drs121913395
GWAS Ctlgrs121913395
Max Magnitude0
ClinVar
Risk rs121913395(A;A)
Alt rs121913395(A;A)
Reference Rs121913395(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene CTNNB1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000003.11:g.41266064G>A
CLNSRC
CLNACC RCV000430055.1,