Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1466535 0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs2074192 0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2026458 0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs702553 0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs877087 0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs879922 0.882 0.160 X 15572684 intron variant C/G snv 4
rs12998782 0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs74577862 0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs113309773 1.000 0.080 16 75398788 intron variant -/A;C ins 0.51 1
rs200495339 1.000 0.080 19 11078623 intron variant G/- delins 0.12 1
rs259140 1.000 0.080 7 89995033 intron variant T/G snv 0.79 1
rs2876300 1.000 0.080 6 12893871 intron variant A/C;G snv 1
rs4675095 1.000 0.080 2 226787251 intron variant A/T snv 5.3E-02 1
rs7265169 1.000 0.080 20 384103 intron variant C/A;T snv 1
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs11413744 1.000 0.080 4 147474132 intergenic variant -/T delins 0.15 1