rs1057519953, RHOA

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.807 0.200 3 49375576 missense variant C/A;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.807 0.200 3 49375576 missense variant C/A;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.807 0.200 3 49375576 missense variant C/A;T snv 0.700 1.000 1 2016 2016
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.807 0.200 3 49375576 missense variant C/A;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.807 0.200 3 49375576 missense variant C/A;T snv 0.700 1.000 1 2016 2016
Adult Burkitt Lymphoma
CUI: C0278764
Disease: Adult Burkitt Lymphoma
7 0.807 0.200 3 49375576 missense variant C/A;T snv 0.010 1.000 1 2014 2014
Burkitt Lymphoma
CUI: C0006413
Disease: Burkitt Lymphoma
13 0.807 0.200 3 49375576 missense variant C/A;T snv 0.010 1.000 1 2014 2014
Childhood Burkitt Lymphoma
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
7 0.807 0.200 3 49375576 missense variant C/A;T snv 0.010 1.000 1 2014 2014