Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs7849782 0.925 0.160 9 101664982 intron variant C/A;G;T snv 3
rs12477677 1.000 0.080 2 207666398 intron variant T/C snv 0.22 2
rs2227288 1.000 0.040 19 8302641 intron variant G/C;T snv 0.12 0.14 2
rs4262994 1.000 0.040 17 37591398 intron variant A/C snv 0.17 2
rs2808635 1 159724419 intergenic variant G/C;T snv 1
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs72554640 0.882 0.160 X 78011239 stop gained C/T snv 9
rs1555889984 0.925 0.120 21 34834536 stop gained C/A snv 5
rs200956636 0.925 0.280 15 55205623 stop gained G/A snv 6.8E-05 6.3E-05 5
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs4149584 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 24
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs1064797245 0.776 0.280 19 41970540 missense variant G/A snv 12
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs28934897
MVK
0.790 0.400 12 109596515 missense variant G/A snv 1.6E-03 1.5E-03 10
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs121918622 0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 9
rs1554785242 0.882 0.160 9 133426240 missense variant G/T snv 8
rs1554791280 0.882 0.160 9 133442718 missense variant T/C snv 8
rs2229291 0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8