Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 6
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 5
rs7372217
ULK4
1.000 0.160 3 41948630 intron variant G/A snv 0.68 4
rs7651190
ULK4
1.000 0.160 3 41724463 intron variant A/G snv 0.33 4
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 4
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 6
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10