rs397507484, 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.
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
82 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 3 2009 2014
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 3 2009 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2013 2013
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.752 0.480 7 140753333 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016