ClinVar
|
Risk
|
rs1057519886(A;A) rs1057519886(C;C) rs1057519886(G;G) |
Alt
|
rs1057519886(A;A) rs1057519886(C;C) rs1057519886(G;G) |
Reference
|
Rs1057519886(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of prostate Hepatocellular carcinoma Malignant melanoma of skin Oesophageal carcinoma Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Adenocarcinoma of lung Adenocarcinoma of stomach Medulloblastoma |
Variation | info |
---|
Gene |
CTNNB1 |
CLNDBN |
Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of prostate Hepatocellular carcinoma Malignant melanoma of skin Oesophageal carcinoma Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Adenocarcinoma of lung Adenocarcinoma of stomach Medulloblastoma |
Reversed |
0 |
HGVS |
NC_000003.11:g.41266100T>A; NC_000003.11:g.41266100T>C; NC_000003.11:g.41266100T>G |
CLNSRC |
|
CLNACC |
RCV000418116.1, RCV000420531.1, RCV000424580.1, RCV000425706.1, RCV000427045.1, RCV000431206.1, RCV000432938.1, RCV000435335.1, RCV000437702.1, RCV000440157.1, RCV000441880.1, RCV000417825.1, RCV000418863.1, RCV000425263.1, RCV000426101.1, RCV000426401.1, RCV000433600.1, RCV000434673.1, RCV000435028.1, RCV000436119.1, RCV000442478.1, RCV000443305.1, RCV000420132.1, RCV000423241.1, RCV000424341.1, RCV000428518.1, RCV000430905.1, RCV000433324.1, RCV000433966.1, RCV000439171.1, RCV000440476.1, RCV000441600.1, RCV000443586.1, |