Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1053321823 1.000 0.160 18 23556404 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1057518942 1.000 0.160 18 23544424 missense variant G/A snv 1
rs1057519242 1.000 0.160 18 23540506 missense variant C/A snv 1
rs1064793791 1.000 0.160 18 23556271 missense variant G/A;C snv 1
rs1160114136 1.000 0.160 18 23540458 stop gained G/A;T snv 4.0E-06 1
rs1191346899 1.000 0.160 18 23539944 missense variant G/A snv 4.0E-06 1
rs120074130 0.925 0.160 18 23539941 missense variant C/T snv 1
rs120074131 0.925 0.160 18 23533470 missense variant C/G;T snv 8.0E-06 1
rs120074132 1.000 0.160 18 23539393 missense variant C/T snv 1.6E-05 1
rs120074134 1.000 0.160 18 23556436 missense variant A/G snv 8.0E-06 1
rs120074135 1.000 0.160 18 23539418 missense variant C/T snv 1.2E-05 1.4E-05 1
rs120074136 1.000 0.160 18 23568949 missense variant A/G snv 1
rs1230538609 1.000 0.160 18 23560369 missense variant C/A;T snv 8.0E-06; 4.0E-06 1
rs1298238512 1.000 0.160 18 23556359 missense variant G/A snv 1
rs1346436537 1.000 0.160 18 23556455 missense variant G/A snv 1.6E-05 1
rs1364834942 1.000 0.160 18 23538627 missense variant C/T snv 1.2E-05 1
rs138184115 1.000 0.160 18 23551720 missense variant C/A;T snv 1.7E-04; 1.2E-05 1
rs1393388896 1.000 0.160 18 23543529 missense variant A/G snv 4.0E-06 1
rs139751448 0.925 0.160 18 23556358 missense variant C/T snv 3.6E-05 7.0E-06 1
rs140211089 1.000 0.160 18 23536871 missense variant T/C snv 4.0E-06 7.0E-06 1
rs1428599096 1.000 0.160 18 23539433 missense variant C/T snv 8.0E-06 7.0E-06 1
rs143124972 0.925 0.160 18 23539447 missense variant G/A snv 1.6E-05 7.0E-06 1
rs150334966 1.000 0.160 18 23538572 missense variant G/A snv 6.8E-04 6.4E-04 1
rs1555631998 1.000 0.160 18 23534534 missense variant C/T snv 1
rs1555632958 1.000 0.160 18 23538596 missense variant A/C snv 1