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
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
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
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv 2
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1150256
IL24
0.925 0.120 1 206899788 intron variant G/A snv 0.40 4
rs11544374
APLNR
1.000 0.040 11 57237103 5 prime UTR variant C/T snv 0.21 2
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs1169089134
FOLH1
0.790 0.320 11 49206785 missense variant C/G;T snv 9
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs11879293
SMARCA4
0.882 0.120 19 10961934 intron variant G/A;C;T snv 4
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12