Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs11067763
LOC105370003
12 115760536 intron variant A/G snv 0.16 3
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs11229457
OR5B12
11 58439730 missense variant C/G;T snv 0.21 0.22 3
rs115236533
CDH18
5 19745606 intron variant G/C snv 3.9E-03 3
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs115795127
FRMD3
9 83378986 intron variant T/C snv 3.4E-02 3
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs11977526
LOC102723446
7 45968511 intron variant G/A;T snv 3
rs12046278
CASZ1
1 10739520 intron variant T/C snv 0.36 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs13143871
GUCY1A1
4 155698052 intron variant T/C snv 0.25 3
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs13175330
PAM
5 102840757 intron variant A/G snv 7.8E-02 2
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1401982
ATP2B1
12 89595822 intron variant G/A snv 0.60 4
rs1563788
ZNF318
6 43340625 intron variant C/T snv 0.42 4