ClinVar
|
Risk
|
rs1057520007(C;C) rs1057520007(G;G) rs1057520007(T;T) |
Alt
|
rs1057520007(C;C) rs1057520007(G;G) rs1057520007(T;T) |
Reference
|
Rs1057520007(A;A) |
Significance |
Probable-Pathogenic |
Disease |
Malignant lymphoma Renal cell carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Neoplasm of breast Pancreatic adenocarcinoma Neoplasm of brain Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Glioblastoma Squamous cell carcinoma of the head and neck Multiple myeloma Oesophageal carcinoma Hepatocellular carcinoma Uterine Carcinosarcoma Colorectal Neoplasms |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Malignant lymphoma, non-Hodgkin Renal cell carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Neoplasm of breast Pancreatic adenocarcinoma Neoplasm of brain Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Glioblastoma Squamous cell carcinoma of the head and neck Multiple myeloma Oesophageal carcinoma Hepatocellular carcinoma Uterine Carcinosarcoma Colorectal Neoplasms |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578235T>A; NC_000017.10:g.7578235T>C; NC_000017.10:g.7578235T>G |
CLNSRC |
|
CLNACC |
RCV000418952.1, RCV000419588.1, RCV000421235.1, RCV000421916.1, RCV000424047.1, RCV000426974.1, RCV000428672.1, RCV000429233.1, RCV000429897.1, RCV000431494.1, RCV000434394.1, RCV000436627.1, RCV000438926.1, RCV000439588.1, RCV000443853.1, RCV000443993.1, RCV000422077.1, RCV000422980.1, RCV000424901.1, RCV000427034.1, RCV000427749.1, RCV000430410.1, RCV000431652.1, RCV000432320.1, RCV000433236.1, RCV000437254.1, RCV000437968.1, RCV000439980.1, RCV000440667.1, RCV000442863.1, RCV000443687.1, RCV000443828.1, RCV000417872.1, RCV000418906.1, RCV000423862.1, RCV000424176.1, RCV000426347.1, RCV000428105.1, RCV000428760.1, RCV000430958.1, RCV000433698.1, RCV000435531.1, RCV000436591.1, RCV000437249.1, RCV000438368.1, RCV000440868.1, RCV000441249.1, RCV000443239.1, |