Source: BEFREE

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: rs4743763
rs4743763
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2019 2019
dbSNP: rs4743763
rs4743763
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2019 2019