Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs17809012
CCL11
0.925 0.160 17 34285425 upstream gene variant A/G;T snv 4
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2301339
CDCA3 ; GNB3
1.000 0.080 12 6845460 3 prime UTR variant G/A;T snv 3
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3