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: rs10738607
rs10738607
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 1.000 1 2007 2018
dbSNP: rs10738607
rs10738607
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.720 1.000 1 2016 2018
dbSNP: rs10738607
rs10738607
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018