rs121913370, BRAF

N. diseases: 10
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.
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 2 2014 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2014 2014
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
30 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 0
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.763 0.360 7 140753393 missense variant T/C;G snv 0.700 0