Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs2306235 0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs57045855 0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs737337 0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs12564445 0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs535039125 0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs13058338 1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs1553265736 0.925 0.040 1 156136080 missense variant G/C snv 4
rs1739843 0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358 0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs61661343 0.851 0.040 1 156130687 missense variant T/C snv 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs1028728 0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs10927887 0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs1249958 0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1258130495 0.882 0.040 4 147485727 missense variant G/A snv 3
rs1303946678 0.925 0.040 22 42126851 missense variant C/G snv 3
rs200536955 0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs3829365 0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11 3
rs6026584 0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs749303395 0.882 0.040 1 114680329 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs794728602 1.000 0.040 1 156115168 missense variant G/A snv 3
rs958546 0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs10932374 0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941 0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2