Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8061882 0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs35441874 0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs36045143 1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs12935657 0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs12924729 0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs12927355 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs34972832 0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2
rs7200786 0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs34069391 0.925 0.080 16 11067358 intron variant T/- delins 2
rs12935413 1.000 0.080 16 11116590 intron variant G/A snv 0.34 2
rs35032408 0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs11644510 1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2
rs11645657 1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 2
rs7203459 1.000 0.080 16 11136846 intron variant T/C snv 0.23 2
rs62026376 0.925 0.120 16 11134855 intron variant C/T snv 0.18 2
rs3862469 1.000 0.040 16 11100223 intron variant C/T snv 0.35 1
rs17806299 1.000 0.080 16 11106123 intron variant G/A snv 0.15 1
rs9923856 1.000 0.080 16 11116558 intron variant T/C snv 0.41 1
rs12708715 1.000 0.080 16 11083967 intron variant C/T snv 0.39 1
rs725613 0.851 0.240 16 11075826 intron variant T/G snv 0.42 1
rs2903692 0.807 0.360 16 11144926 intron variant G/A snv 0.33 1
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 1
rs887864 0.925 0.120 16 11065028 intron variant G/A;C;T snv 1
rs248831 16 11187361 intergenic variant G/A snv 0.31 1
rs2041670 0.851 0.280 16 11080795 intron variant G/A;C snv 1