ClinVar
|
Risk
|
rs1057519981(C;C) rs1057519981(G;G) |
Alt
|
rs1057519981(C;C) rs1057519981(G;G) |
Reference
|
Rs1057519981(T;T) |
Significance |
Pathogenic |
Disease |
Adenocarcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Uterine cervical neoplasms Transitional cell carcinoma of the bladder Colorectal Neoplasms Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Multiple myeloma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Neoplasm of brain Hepatocellular carcinoma Hereditary cancer-predisposing syndrome |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Adenocarcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Uterine cervical neoplasms Transitional cell carcinoma of the bladder Colorectal Neoplasms Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Chronic lymphocytic leukemia Multiple myeloma Malignant neoplasm of body of uterus Squamous cell carcinoma of the head and neck Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Neoplasm of brain Hepatocellular carcinoma Hereditary cancer-predisposing syndrome |
Reversed |
1 |
HGVS |
NC_000017.10:g.7577569A>C; NC_000017.10:g.7577569A>G |
CLNSRC |
|
CLNACC |
RCV000417486.1, RCV000420677.1, RCV000422044.1, RCV000422283.1, RCV000423396.1, RCV000427246.1, RCV000428630.1, RCV000428804.1, RCV000430919.1, RCV000433478.1, RCV000435170.1, RCV000437321.1, RCV000437476.1, RCV000438876.1, RCV000439946.1, RCV000443356.1, RCV000444792.1, RCV000419348.1, RCV000420409.1, RCV000421679.1, RCV000421933.1, RCV000424052.1, RCV000426193.1, RCV000428210.1, RCV000430482.1, RCV000430655.1, RCV000431946.1, RCV000433046.1, RCV000437018.1, RCV000437199.1, RCV000438447.1, RCV000441834.1, RCV000441879.1, RCV000442237.1, RCV000492666.1, |