rs28931589

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs28931589(G;T)

Make rs28931589(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

41224613

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs28931589
dbSNP (classic)	rs28931589
ClinGen	rs28931589
ebi	rs28931589
HLI	rs28931589
Exac	rs28931589
Gnomad	rs28931589
Varsome	rs28931589
LitVar	rs28931589
Map	rs28931589
PheGenI	rs28931589
Biobank	rs28931589
1000 genomes	rs28931589
hgdp	rs28931589
ensembl	rs28931589
geneview	rs28931589
scholar	rs28931589
google	rs28931589
pharmgkb	rs28931589
gwascentral	rs28931589
openSNP	rs28931589
23andMe	rs28931589
SNPshot	rs28931589
SNPdbe	rs28931589
MSV3d	rs28931589
GWAS Ctlg	rs28931589

Max Magnitude

0

NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP

OMIM	116806
Desc	HEPATOBLASTOMA, SOMATIC
Variant	0005
Related	also

OMIM	116806
Desc
Variant	0008
Related	also

ClinVar
Risk	rs28931589(A;A) rs28931589(C;C) rs28931589(T;T)
Alt	rs28931589(A;A) rs28931589(C;C) rs28931589(T;T)
Reference	Rs28931589(G;G)
Significance	Pathogenic
Disease	Pilomatrixoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Ovarian Neoplasms Adrenocortical carcinoma Malignant neoplasm of body of uterus Malignant melanoma of skin Adenocarcinoma of lung Hepatocellular carcinoma Medulloblastoma Hepatoblastoma Malignant tumor of prostate Craniopharyngioma Malignant melanoma
Variation	info
Gene	CTNNB1
CLNDBN	Pilomatrixoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Ovarian Neoplasms Adrenocortical carcinoma Malignant neoplasm of body of uterus Malignant melanoma of skin Adenocarcinoma of lung Hepatocellular carcinoma Medulloblastoma Hepatoblastoma Malignant tumor of prostate Craniopharyngioma Malignant melanoma
Reversed	0
HGVS	NC_000003.11:g.41266104G>A; NC_000003.11:g.41266104G>C; NC_000003.11:g.41266104G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019149.5, RCV000422250.1, RCV000423249.1, RCV000426491.1, RCV000432939.1, RCV000433938.1, RCV000434538.1, RCV000439589.1, RCV000443851.1, RCV000443977.1, RCV000419447.1, RCV000427084.1, RCV000427731.1, RCV000430157.1, RCV000436689.1, RCV000437750.1, RCV000442160.1, RCV000442184.1, RCV000019146.5, RCV000149120.1, RCV000417805.1, RCV000418024.1, RCV000418475.1, RCV000425225.1, RCV000427137.1, RCV000428985.1, RCV000429363.1, RCV000435058.1, RCV000436574.1, RCV000437867.1,

[PMID 19635198] [Correlation of genetic polymorphisms of beta-catenin to hepatitis B virus-related hepatocellular carcinoma].