Disease: Mean blood pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6