Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1452075 1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs1553518509 1.000 0.040 2 148468916 stop gained C/T snv 2
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs526126 1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 2
rs10497655 1.000 0.040 2 184597314 intron variant T/C;G snv 1
rs10498676 0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs121908445 0.925 0.040 7 148147542 missense variant T/C snv 3.3E-04 1.7E-04 1
rs1276388879 1.000 0.040 1 151405647 missense variant A/C;G snv 1
rs1372713010 1.000 0.040 1 151428041 missense variant G/A snv 1
rs1396313317 1.000 0.040 7 147562137 splice acceptor variant G/A;C snv 4.0E-06 1
rs1418634444 1.000 0.040 1 151408777 missense variant T/C snv 7.0E-06 1
rs1452048149 1.000 0.040 1 151404828 missense variant C/T snv 4.0E-06 1
rs1476293577 1.000 0.040 1 151428188 missense variant G/A;C snv 1
rs1484207450 1.000 0.040 1 151405155 missense variant A/G snv 7.0E-06 1
rs1557863430 1.000 0.040 1 151405229 missense variant T/C snv 1
rs1557863440 1.000 0.040 1 151405233 missense variant T/C snv 1
rs1557863546 1.000 0.040 1 151405263 missense variant T/A snv 1
rs1557867853 1.000 0.040 1 151406330 missense variant G/A snv 1
rs1557870645 1.000 0.040 1 151407271 missense variant C/T snv 1
rs1557874046 1.000 0.040 1 151408807 missense variant T/G snv 1
rs1557901347 1.000 0.040 1 151424027 missense variant G/C snv 1
rs1557902023 1.000 0.040 1 151424154 missense variant G/C snv 1