Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs4953354
EPAS1
0.827 0.120 2 46348249 intron variant A/G snv 0.22 5
rs1868092
EPAS1
1.000 0.040 2 46387063 downstream gene variant G/A snv 0.34 4
rs12619696 1.000 0.040 2 46463303 intron variant G/A snv 0.15 1
rs2478523
AGT
1.000 0.040 1 230705763 intron variant A/G snv 0.50 1
rs141267844
ERBB4
1.000 0.040 2 211430865 intron variant -/T delins 0.32 1
rs6710946
ERBB4
1.000 0.040 2 211431150 intron variant C/T snv 0.73 0.78 1
rs934607
ERBB4
1.000 0.040 2 211388084 intron variant G/A snv 0.63 1
rs3749148
ITGA6-AS1 ; ITGA6
1.000 0.040 2 172465821 splice region variant T/G snv 0.16 1
rs3813865
LOC107984284 ; CYP2E1
1.000 0.040 10 133525740 intron variant G/C snv 6.9E-02 1