Source: GWASCAT

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: rs1250259
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs17517928
rs17517928
FN1
1.000 0.040 2 215426636 intron variant C/T snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2017 2017