Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs769581210 1.000 0.040 1 151405376 missense variant T/C snv 7.2E-05 3.5E-05 1
rs202098093 1.000 0.040 1 151405476 missense variant G/A snv 1.2E-05 7.0E-06 1
rs1276388879 1.000 0.040 1 151405647 missense variant A/C;G snv 1
rs760211123 1.000 0.040 1 151405662 missense variant T/C snv 1.2E-05 7.0E-06 1
rs778792467 1.000 0.040 1 151405692 missense variant G/C snv 4.4E-05 7.0E-06 1
rs760059077 1.000 0.040 1 151405919 missense variant C/T snv 2.4E-05 2.1E-05 1
rs373783340 1.000 0.040 1 151406243 missense variant G/A snv 4.0E-05 1.2E-04 1
rs1557867853 1.000 0.040 1 151406330 missense variant G/A snv 1
rs772572695 1.000 0.040 1 151406427 missense variant C/A;T snv 2.5E-05 1
rs753214391 1.000 0.040 1 151406444 missense variant C/T snv 1.0E-05 2.1E-05 1
rs749270162 1.000 0.040 1 151406620 missense variant T/C snv 2.4E-05 1
rs548226228 1.000 0.040 1 151406914 missense variant G/A snv 1.2E-05 2.1E-05 1
rs1557870645 1.000 0.040 1 151407271 missense variant C/T snv 1
rs1418634444 1.000 0.040 1 151408777 missense variant T/C snv 7.0E-06 1
rs1557874046 1.000 0.040 1 151408807 missense variant T/G snv 1
rs749548928 1.000 0.040 1 151408815 missense variant T/C;G snv 4.0E-06 1
rs754532606 1.000 0.040 1 151423526 missense variant C/T snv 8.0E-06 2.1E-05 1
rs1557901347 1.000 0.040 1 151424027 missense variant G/C snv 1
rs763820362 1.000 0.040 1 151424045 missense variant C/T snv 2.4E-05 1
rs888864913 1.000 0.040 1 151424097 missense variant C/T snv 1.2E-05 2.8E-05 1
rs1557902023 1.000 0.040 1 151424154 missense variant G/C snv 1
rs574158925 1.000 0.040 1 151427829 missense variant T/C snv 5.6E-05 2.8E-05 1
rs1557909572 1.000 0.040 1 151427931 missense variant G/C snv 1