Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5335
EDNRA
0.925 0.120 4 147542688 3 prime UTR variant G/A;C snv 3
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs768349387
ADRB2
1.000 0.080 5 148827850 missense variant T/C snv 8.0E-06 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs866528738
POU2F3
1.000 0.080 11 120302360 missense variant G/A snv 2
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs796145467
LDLR
0.925 0.080 19 11123310 synonymous variant C/T snv 4.0E-06 2.1E-05 3
rs147783135
TMPRSS7
1.000 0.080 3 112081004 stop gained C/T snv 2.4E-04 6.3E-05 3
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs191885206
CYP4F12
1.000 0.080 19 15696024 missense variant T/C snv 7.0E-04 3.1E-04 3
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs2230500
PRKCH
0.925 0.080 14 61457521 missense variant G/A snv 3.1E-02 1.6E-02 5
rs5355
C1orf112 ; SELE
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14