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rs121913228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913228(G;G)
Make rs121913228(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224621
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913228
dbSNP (old)rs121913228
ClinGenrs121913228
ebirs121913228
HLIrs121913228
Exacrs121913228
Gnomadrs121913228
Varsomers121913228
LitVarrs121913228
Maprs121913228
PheGenIrs121913228
Biobankrs121913228
1000 genomesrs121913228
hgdprs121913228
ensemblrs121913228
gopubmedrs121913228
geneviewrs121913228
scholarrs121913228
googlers121913228
pharmgkbrs121913228
gwascentralrs121913228
openSNPrs121913228
23andMers121913228
23andMe allrs121913228
SNPshotrs121913228
SNPdbers121913228
MSV3drs121913228
GWAS Ctlgrs121913228
Max Magnitude0
ClinVar
Risk rs121913228(C;C) rs121913228(G;G)
Alt rs121913228(C;C) rs121913228(G;G)
Reference Rs121913228(T;T)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of stomach Hepatocellular carcinoma Adenocarcinoma of prostate Adenocarcinoma of lung Medulloblastoma Adenocarcinoma of stomach Uterine cervical neoplasms Oesophageal carcinoma Parathyroid gland neoplasm
Variation info
Gene CTNNB1
CLNDBN Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of stomach Hepatocellular carcinoma Adenocarcinoma of prostate Adenocarcinoma of lung Medulloblastoma Adenocarcinoma of stomach Uterine cervical neoplasms Oesophageal carcinoma Parathyroid gland neoplasm
Reversed 0
HGVS NC_000003.11:g.41266112T>C; NC_000003.11:g.41266112T>G
CLNSRC
CLNACC RCV000423296.1, RCV000423766.1, RCV000423953.1, RCV000429643.1, RCV000431861.1, RCV000434676.1, RCV000440333.1, RCV000440535.1, RCV000443827.1, RCV000444541.1, RCV000419464.1, RCV000419658.1, RCV000424491.1, RCV000426018.1, RCV000430355.1, RCV000430984.1, RCV000435198.1, RCV000435831.1, RCV000436705.1, RCV000444358.1,