Disease: Heart failure
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19