Disease: Hypertensive disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
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
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs11097432
PDLIM5
1.000 0.080 4 94658554 intron variant T/C snv 0.24 2
rs1150256
IL24
0.925 0.120 1 206899788 intron variant G/A snv 0.40 4
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 5
rs12576239
KCNQ1
1.000 0.080 11 2481089 intron variant C/T snv 0.16 3
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13306519
LEPR
1.000 0.080 1 65572246 intron variant C/G;T snv 2
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10