rs121913361, BRAF

N. diseases: 6
Source: CLINVAR ×
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
216 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 7 2002 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
211 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
115 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
129 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
76 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
141 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016