Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.700 1.000 3 2009 2014
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		0.700 1.000 3 2009 2014
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2013 2013
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2016 2016
dbSNP: rs397507484
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate 		0.700 1.000 1 2016 2016