rs121913228

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121913228(G;G)

Make rs121913228(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

41224621

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs121913228
dbSNP (classic)	rs121913228
ClinGen	rs121913228
ebi	rs121913228
HLI	rs121913228
Exac	rs121913228
Gnomad	rs121913228
Varsome	rs121913228
LitVar	rs121913228
Map	rs121913228
PheGenI	rs121913228
Biobank	rs121913228
1000 genomes	rs121913228
hgdp	rs121913228
ensembl	rs121913228
geneview	rs121913228
scholar	rs121913228
google	rs121913228
pharmgkb	rs121913228
gwascentral	rs121913228
openSNP	rs121913228
23andMe	rs121913228
SNPshot	rs121913228
SNPdbe	rs121913228
MSV3d	rs121913228
GWAS Ctlg	rs121913228

Max Magnitude

0

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,