ClinVar
|
Risk
|
rs1057520008(A;A) rs1057520008(C;C) rs1057520008(G;G) |
Alt
|
rs1057520008(A;A) rs1057520008(C;C) rs1057520008(G;G) |
Reference
|
Rs1057520008(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Pancreatic adenocarcinoma Adenocarcinoma of lung Multiple myeloma Malignant lymphoma Renal cell carcinoma Neoplasm of breast Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Hepatocellular carcinoma Neoplasm of brain Malignant neoplasm of body of uterus Colorectal Neoplasms Squamous cell carcinoma of lung Oesophageal carcinoma Glioblastoma Li-Fraumeni syndrome |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Pancreatic adenocarcinoma Adenocarcinoma of lung Multiple myeloma Malignant lymphoma, non-Hodgkin Renal cell carcinoma Neoplasm of breast Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Uterine Carcinosarcoma Hepatocellular carcinoma Neoplasm of brain Malignant neoplasm of body of uterus Colorectal Neoplasms Squamous cell carcinoma of lung Oesophageal carcinoma Glioblastoma Li-Fraumeni syndrome |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578236A>C; NC_000017.10:g.7578236A>G; NC_000017.10:g.7578236A>T |
CLNSRC |
|
CLNACC |
RCV000419128.1, RCV000421137.1, RCV000421350.1, RCV000423676.1, RCV000426948.1, RCV000428535.1, RCV000428939.1, RCV000430021.1, RCV000434351.1, RCV000434446.1, RCV000436740.1, RCV000438356.1, RCV000439629.1, RCV000439865.1, RCV000444122.1, RCV000444873.1, RCV000462351.1, RCV000419308.1, RCV000420368.1, RCV000421826.1, RCV000422887.1, RCV000424493.1, RCV000426781.1, RCV000427755.1, RCV000431739.1, RCV000431958.1, RCV000432726.1, RCV000437451.1, RCV000437587.1, RCV000439923.1, RCV000440094.1, RCV000443622.1, RCV000443753.1, RCV000417461.1, RCV000419577.1, RCV000420753.1, RCV000422784.1, RCV000424682.1, RCV000424892.1, RCV000426051.1, RCV000430294.1, RCV000430575.1, RCV000432365.1, RCV000433474.1, RCV000435608.1, RCV000437987.1, RCV000441202.1, RCV000444287.1, RCV000444368.1, |