rs28931588

Orientation

plus

Stabilized

plus

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

Make rs28931588(G;T)

Make rs28931588(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

41224606

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs28931588
dbSNP (classic)	rs28931588
ClinGen	rs28931588
ebi	rs28931588
HLI	rs28931588
Exac	rs28931588
Gnomad	rs28931588
Varsome	rs28931588
LitVar	rs28931588
Map	rs28931588
PheGenI	rs28931588
Biobank	rs28931588
1000 genomes	rs28931588
hgdp	rs28931588
ensembl	rs28931588
geneview	rs28931588
scholar	rs28931588
google	rs28931588
pharmgkb	rs28931588
gwascentral	rs28931588
openSNP	rs28931588
23andMe	rs28931588
SNPshot	rs28931588
SNPdbe	rs28931588
MSV3d	rs28931588
GWAS Ctlg	rs28931588

Max Magnitude

0

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

OMIM	116806
Desc	HEPATOBLASTOMA, SOMATIC
Variant	0004
Related	also

OMIM	116806
Desc	PILOMATRICOMA, SOMATIC
Variant	0016
Related	also

ClinVar
Risk	rs28931588(A;A) rs28931588(C;C) rs28931588(T;T)
Alt	rs28931588(A;A) rs28931588(C;C) rs28931588(T;T)
Reference	Rs28931588(G;G)
Significance	Pathogenic
Disease	Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Medulloblastoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Esophageal Squamous Cell Carcinoma Endometrial neoplasm Uterine cervical neoplasms Malignant melanoma Hepatoblastoma Pilomatrixoma Craniopharyngioma
Variation	info
Gene	CTNNB1
CLNDBN	Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Medulloblastoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Esophageal Squamous Cell Carcinoma Endometrial neoplasm Uterine cervical neoplasms Malignant melanoma Hepatoblastoma Pilomatrixoma Craniopharyngioma
Reversed	0
HGVS	NC_000003.11:g.41266097G>A; NC_000003.11:g.41266097G>C; NC_000003.11:g.41266097G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000421306.1, RCV000423696.1, RCV000425710.1, RCV000431551.1, RCV000432187.1, RCV000432497.1, RCV000438971.1, RCV000441401.1, RCV000444118.1, RCV000444402.1, RCV000419510.1, RCV000421744.1, RCV000422380.1, RCV000429157.1, RCV000429774.1, RCV000430427.1, RCV000437131.1, RCV000439366.1, RCV000440025.1, RCV000019144.3, RCV000128842.6, RCV000418154.1, RCV000419388.1, RCV000420526.1, RCV000426162.1, RCV000426839.1, RCV000430774.1, RCV000437074.1, RCV000438170.1, RCV000441036.1,

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