ClinVar
|
Risk
|
rs876660333(A;A) rs876660333(G;G) |
Alt
|
rs876660333(A;A) rs876660333(G;G) |
Reference
|
Rs876660333(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Hereditary cancer-predisposing syndrome Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of breast Multiple myeloma Colorectal Neoplasms Pancreatic adenocarcinoma Adenocarcinoma of lung Renal cell carcinoma Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Medulloblastoma |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Hereditary cancer-predisposing syndrome Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of breast Multiple myeloma Colorectal Neoplasms Pancreatic adenocarcinoma Adenocarcinoma of lung Renal cell carcinoma Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Medulloblastoma |
Reversed |
1 |
HGVS |
NC_000017.10:g.7577123A>C; NC_000017.10:g.7577123A>T |
CLNSRC |
|
CLNACC |
RCV000220536.1, RCV000419845.1, RCV000420090.1, RCV000421184.1, RCV000421439.1, RCV000422297.1, RCV000427960.1, RCV000430105.1, RCV000431226.1, RCV000432569.1, RCV000439065.1, RCV000441216.1, RCV000441467.1, RCV000444129.1, RCV000421804.1, RCV000422825.1, RCV000423493.1, RCV000424786.1, RCV000427639.1, RCV000429369.1, RCV000433521.1, RCV000434183.1, RCV000438331.1, RCV000440060.1, RCV000442761.1, RCV000442953.1, RCV000444340.1, |