ClinVar
|
Risk
|
rs1057519978(A;A) rs1057519978(C;C) rs1057519978(G;G) |
Alt
|
rs1057519978(A;A) rs1057519978(C;C) rs1057519978(G;G) |
Reference
|
Rs1057519978(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Acute myeloid leukemia Colorectal Neoplasms Adenocarcinoma of lung Multiple myeloma Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Neoplasm of breast Renal cell carcinoma Adenocarcinoma of prostate Squamous cell carcinoma of lung Neoplasm of brain |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Acute myeloid leukemia Colorectal Neoplasms Adenocarcinoma of lung Multiple myeloma Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Neoplasm of breast Renal cell carcinoma Adenocarcinoma of prostate Squamous cell carcinoma of lung Neoplasm of brain |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578509A>C; NC_000017.10:g.7578509A>G; NC_000017.10:g.7578509A>T |
CLNSRC |
|
CLNACC |
RCV000419137.1, RCV000420961.1, RCV000425541.1, RCV000426677.1, RCV000427661.1, RCV000432339.1, RCV000432969.1, RCV000436820.1, RCV000437911.1, RCV000438636.1, RCV000444521.1, RCV000444835.1, RCV000418678.1, RCV000419723.1, RCV000420817.1, RCV000423623.1, RCV000425407.1, RCV000430017.1, RCV000431037.1, RCV000432161.1, RCV000436190.1, RCV000437414.1, RCV000440220.1, RCV000441312.1, RCV000417913.1, RCV000420314.1, RCV000421892.1, RCV000422574.1, RCV000428237.1, RCV000430556.1, RCV000432852.1, RCV000433900.1, RCV000438490.1, RCV000439057.1, RCV000439533.1, RCV000442038.1, |