Geno
|
Mag
|
Summary
|
(G;G)
|
0
|
common in complete genomics
|
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
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].