Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9