Disease: Mean blood pressure
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 8
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 8
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs13002573 2 164058698 intron variant A/G snv 0.20 3
rs1327235 20 10988382 intron variant A/G snv 0.46 6
rs16982520
ZNF831
1.000 0.040 20 59183665 intron variant A/G snv 0.14 4
rs17037452
CLCN6
1 11835618 intron variant A/G snv 0.18 3
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 7
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs4714678 6 43374853 intron variant A/G snv 0.45 2
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5