Disease: Heart failure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16