Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10411210 0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs10883782 0.925 0.080 10 102824175 intron variant A/G snv 0.14 2
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs115797771 0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs118049207 0.925 0.080 7 127890817 intron variant A/G snv 1.7E-03 2
rs11874392 0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12037879 0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12477554 0.925 0.080 2 75174939 intron variant A/G;T snv 2
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs12953717 0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs1329149 0.925 0.080 10 133536297 intron variant T/C snv 0.73 2
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs17026425 0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs1725459 0.925 0.080 19 38049092 intron variant C/A;G;T snv 2