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rs121913399

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913399(A;A)
Make rs121913399(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224612
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913399
dbSNP (old)rs121913399
ClinGenrs121913399
ebirs121913399
HLIrs121913399
Exacrs121913399
Gnomadrs121913399
Varsomers121913399
Maprs121913399
PheGenIrs121913399
Biobankrs121913399
1000 genomesrs121913399
hgdprs121913399
ensemblrs121913399
gopubmedrs121913399
geneviewrs121913399
scholarrs121913399
googlers121913399
pharmgkbrs121913399
gwascentralrs121913399
openSNPrs121913399
23andMers121913399
23andMe allrs121913399
SNPshotrs121913399
SNPdbers121913399
MSV3drs121913399
GWAS Ctlgrs121913399
Max Magnitude0
ClinVar
Risk rs121913399(A;A) rs121913399(C;C)
Alt rs121913399(A;A) rs121913399(C;C)
Reference Rs121913399(G;G)
Significance Probable-Pathogenic
Disease Craniopharyngioma Pilomatrixoma Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Malignant melanoma of skin Adenocarcinoma of lung Malignant neoplasm of body of uterus Medulloblastoma Adrenocortical carcinoma
Variation info
Gene CTNNB1
CLNDBN Craniopharyngioma Pilomatrixoma Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Malignant melanoma of skin Adenocarcinoma of lung Malignant neoplasm of body of uterus Medulloblastoma Adrenocortical carcinoma
Reversed 0
HGVS NC_000003.11:g.41266103G>A; NC_000003.11:g.41266103G>C
CLNSRC
CLNACC RCV000426895.1, RCV000444074.1, RCV000418083.1, RCV000419419.1, RCV000420040.1, RCV000427501.1, RCV000427907.1, RCV000430713.1, RCV000436663.1, RCV000438184.1, RCV000438599.1, RCV000438776.1,