Disease: Hypertensive disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3