ClinVar
|
Risk
|
rs1057519895(A;A) rs1057519895(C;C) rs1057519895(T;T) |
Alt
|
rs1057519895(A;A) rs1057519895(C;C) rs1057519895(T;T) |
Reference
|
Rs1057519895(G;G) |
Significance |
Probable-Pathogenic |
Disease |
Adenocarcinoma of stomach Squamous cell carcinoma of lung Adenoid cystic carcinoma Uterine Carcinosarcoma Malignant neoplasm of body of uterus Oesophageal carcinoma Squamous cell carcinoma of the head and neck Medulloblastoma Chronic lymphocytic leukemia Neoplasm of breast Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Uterine cervical neoplasms |
Variation | info |
---|
Gene |
FBXW7 |
CLNDBN |
Adenocarcinoma of stomach Squamous cell carcinoma of lung Adenoid cystic carcinoma Uterine Carcinosarcoma Malignant neoplasm of body of uterus Oesophageal carcinoma Squamous cell carcinoma of the head and neck Medulloblastoma Chronic lymphocytic leukemia Neoplasm of breast Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Uterine cervical neoplasms |
Reversed |
1 |
HGVS |
NC_000004.11:g.153249384C>A; NC_000004.11:g.153249384C>G; NC_000004.11:g.153249384C>T |
CLNSRC |
|
CLNACC |
RCV000419727.1, RCV000421731.1, RCV000422964.1, RCV000423635.1, RCV000425901.1, RCV000430408.1, RCV000431029.1, RCV000431539.1, RCV000434382.1, RCV000436100.1, RCV000440224.1, RCV000441781.1, RCV000443518.1, RCV000443662.1, RCV000417428.1, RCV000418970.1, RCV000422698.1, RCV000424610.1, RCV000424801.1, RCV000427741.1, RCV000428799.1, RCV000433446.1, RCV000434066.1, RCV000435527.1, RCV000436201.1, RCV000440831.1, RCV000442912.1, RCV000443932.1, RCV000417744.1, RCV000417975.1, RCV000420844.1, RCV000422069.1, RCV000426392.1, RCV000427168.1, RCV000428675.1, RCV000429314.1, RCV000433642.1, RCV000437827.1, RCV000437932.1, RCV000438452.1, RCV000439989.1, RCV000443195.1, |