Disease: Cardiovascular Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5