Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10498676 0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs1131692040 0.882 0.160 X 154399844 missense variant A/G snv 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
rs1418634444 1.000 0.040 1 151408777 missense variant T/C snv 7.0E-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
rs1557909572 1.000 0.040 1 151427931 missense variant G/C snv 1
rs1557909821 1.000 0.040 1 151427999 missense variant A/G snv 1
rs1557910728 1.000 0.040 1 151428233 missense variant T/C snv 1
rs1557911386 1.000 0.040 1 151428357 missense variant T/A snv 1
rs1557916296 1.000 0.040 1 151430822 missense variant C/A snv 1
rs1557935477 1.000 0.040 1 151440939 missense variant G/T snv 1
rs1561824498 1.000 0.040 5 88752044 splice acceptor variant C/A snv 1
rs1564801388 1.000 0.040 10 87864353 5 prime UTR variant -/G delins 1
rs1564801473 1.000 0.040 10 87864406 5 prime UTR variant -/C delins 1
rs1564950387 1.000 0.040 11 687909 splice donor variant A/C snv 1