ClinVar
|
Risk
|
rs1057519990(C;C) |
Alt
|
rs1057519990(C;C) |
Reference
|
Rs1057519990(G;G) |
Significance |
Probable-Pathogenic |
Disease |
Glioblastoma Adenocarcinoma of lung Neoplasm of breast Colorectal Neoplasms Malignant melanoma of skin Ovarian Serous Cystadenocarcinoma Oesophageal carcinoma Transitional cell carcinoma of the bladder Neoplasm of brain Uterine Carcinosarcoma Squamous cell carcinoma of the skin Squamous cell carcinoma of lung Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Pancreatic adenocarcinoma Hepatocellular carcinoma Small cell lung cancer |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Glioblastoma Adenocarcinoma of lung Neoplasm of breast Colorectal Neoplasms Malignant melanoma of skin Ovarian Serous Cystadenocarcinoma Oesophageal carcinoma Transitional cell carcinoma of the bladder Neoplasm of brain Uterine Carcinosarcoma Squamous cell carcinoma of the skin Squamous cell carcinoma of lung Chronic lymphocytic leukemia Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Pancreatic adenocarcinoma Hepatocellular carcinoma Small cell lung cancer |
Reversed |
1 |
HGVS |
NC_000017.10:g.7577142C>G |
CLNSRC |
|
CLNACC |
RCV000419323.1, RCV000419956.1, RCV000420436.1, RCV000421105.1, RCV000422610.1, RCV000425613.1, RCV000426755.1, RCV000426767.1, RCV000430688.1, RCV000431342.1, RCV000431795.1, RCV000432420.1, RCV000435860.1, RCV000437000.1, RCV000439191.1, RCV000439845.1, RCV000441587.1, RCV000444661.1, |