Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1567438
LPAL2
0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2746071
RGS2
0.882 0.160 1 192808434 intron variant A/G snv 0.35 4
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 4
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7