Source: GWASDB

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: rs12231737
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.700 1.000 1 2011 2011
dbSNP: rs12231737
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2013 2013
dbSNP: rs17630235
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs17630235
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17630235
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013