rs121913365, 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.
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2014 2014
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.776 0.320 7 140753332 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Hematochezia
CUI: C0018932
Disease: Hematochezia
12 0.776 0.320 7 140753332 missense variant T/A;G snv 0.010 1.000 1 2004 2004
Pain
CUI: C0030193
Disease: Pain
196 0.776 0.320 7 140753332 missense variant T/A;G snv 0.010 1.000 1 2004 2004