ClinVar
|
Risk
|
rs1057520003(C;C) |
Alt
|
rs1057520003(C;C) |
Reference
|
Rs1057520003(A;A) |
Significance |
Probable-Pathogenic |
Disease |
Colorectal Neoplasms Squamous cell carcinoma of the head and neck Transitional cell carcinoma of the bladder Malignant melanoma of skin Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Brainstem glioma Small cell lung cancer Neoplasm of brain Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Hepatocellular carcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Renal cell carcinoma Adrenocortical carcinoma Squamous cell carcinoma of lung Oesophageal carcinoma Pancreatic adenocarcinoma |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Colorectal Neoplasms Squamous cell carcinoma of the head and neck Transitional cell carcinoma of the bladder Malignant melanoma of skin Neoplasm of breast Glioblastoma Adenocarcinoma of stomach Brainstem glioma Small cell lung cancer Neoplasm of brain Acute myeloid leukemia Ovarian Serous Cystadenocarcinoma Hepatocellular carcinoma Squamous cell carcinoma of the skin Adenocarcinoma of lung Renal cell carcinoma Adrenocortical carcinoma Squamous cell carcinoma of lung Oesophageal carcinoma Pancreatic adenocarcinoma |
Reversed |
1 |
HGVS |
NC_000017.10:g.7579314T>G |
CLNSRC |
|
CLNACC |
RCV000417666.1, RCV000418295.1, RCV000422630.1, RCV000423200.1, RCV000425049.1, RCV000426486.1, RCV000427158.1, RCV000428307.1, RCV000429194.1, RCV000432449.1, RCV000433906.1, RCV000434566.1, RCV000434887.1, RCV000436394.1, RCV000437835.1, RCV000439620.1, RCV000439813.1, RCV000442101.1, RCV000442185.1, RCV000443332.1, |