Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201518227 1.000 1 179917914 missense variant C/T snv 3.2E-05 5.6E-05 13
rs121434591 1.000 5 139307669 missense variant C/G snv 5
rs17601696 10 121360522 intergenic variant C/T snv 6.0E-02 2
rs202102815 17 63941396 missense variant G/A;T snv 1.5E-04; 8.0E-06 1
rs1334099693 0.882 0.080 6 21594732 missense variant C/A;T snv 4.6E-06 11
rs10835211 1.000 0.080 11 27679818 intron variant G/A snv 0.19 3
rs781565158 0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 22
rs1566785990 0.851 0.120 14 77026534 missense variant A/G snv 12
rs73956431 0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs1553475005 1.000 0.120 2 174824485 missense variant A/G snv 4
rs139632595 0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 19
rs797044849 0.807 0.160 12 13567164 missense variant C/A;G;T snv 4.0E-06 17
rs137852959 0.790 0.160 20 3918695 missense variant G/A snv 8.7E-05 2.3E-04 9
rs28937581 0.827 0.160 2 71570300 missense variant G/T snv 1.2E-05 9
rs2949506 0.851 0.160 18 30217168 intergenic variant C/T snv 0.14 5
rs63750687 0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs140226130 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs10163755 0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs1448259271 0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs1064796765 0.763 0.240 14 102002950 missense variant G/A snv 19
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17
rs1555968941 0.752 0.280 12 2653847 missense variant G/A;C snv 31
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27