Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12124383 1.000 0.080 1 155946002 downstream gene variant G/A snv 3.7E-03 2
rs12490383
SCAP
1.000 0.080 3 47452667 intron variant T/C snv 0.14 2
rs2002880
IGF1R
1.000 0.080 15 98960516 3 prime UTR variant G/A snv 3.6E-03 2
rs2289277
TSLP
1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs3748024
CHCHD5
0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs6219
HELLPAR ; LINC02456 ; IGF1
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02 2
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs1269801977
PPIG
0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 4
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs1805081
NPC1
0.925 0.120 18 23560468 missense variant T/C snv 0.33 0.29 3
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs568401628
ACE
0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 4
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs225015
DIO2
0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18