ClinVar
|
Risk
|
rs149680468(A;A) rs149680468(C;C) rs149680468(T;T) |
Alt
|
rs149680468(A;A) rs149680468(C;C) rs149680468(T;T) |
Reference
|
Rs149680468(G;G) |
Significance |
Probable-Pathogenic |
Disease |
Malignant neoplasm of body of uterus Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Uterine Carcinosarcoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Oesophageal carcinoma Colorectal Neoplasms Malignant melanoma of skin Chronic lymphocytic leukemia Uterine cervical neoplasms |
Variation | info |
---|
Gene |
FBXW7 |
CLNDBN |
Malignant neoplasm of body of uterus Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of lung Transitional cell carcinoma of the bladder Uterine Carcinosarcoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Oesophageal carcinoma Colorectal Neoplasms Malignant melanoma of skin Chronic lymphocytic leukemia Uterine cervical neoplasms |
Reversed |
0 |
HGVS |
NC_000004.11:g.153247289G>A; NC_000004.11:g.153247289G>C; NC_000004.11:g.153247289G>T |
CLNSRC |
|
CLNACC |
RCV000422076.1, RCV000422275.1, RCV000426925.1, RCV000427176.1, RCV000428536.1, RCV000432318.1, RCV000433395.1, RCV000437170.1, RCV000438775.1, RCV000443061.1, RCV000444088.1, RCV000444218.1, RCV000419644.1, RCV000420774.1, RCV000420999.1, RCV000425337.1, RCV000426495.1, RCV000430756.1, RCV000431005.1, RCV000436496.1, RCV000437332.1, RCV000437528.1, RCV000438652.1, RCV000443509.1, RCV000419073.1, RCV000419711.1, RCV000420985.1, RCV000423791.1, RCV000429788.1, RCV000430339.1, RCV000431685.1, RCV000434480.1, RCV000440442.1, RCV000441048.1, RCV000441739.1, RCV000444420.1, |