rs121913355, BRAF

N. diseases: 4
Source: UNIPROT ×
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.
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
19 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 4 2006 2009
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
4 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 1 2003 2003
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
41 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.700 0
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
11 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.700 0