Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 7
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 2