Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060499900 0.925 0.080 3 38551304 missense variant C/T snv 4.0E-06 1.4E-05 2
rs12720452 0.882 0.120 3 38603758 missense variant C/T snv 2.9E-04 2.9E-04 5
rs137854600 0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs137854602 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs137854603 1.000 0.080 3 38550602 missense variant C/T snv 6.0E-05 2.8E-05 1
rs137854604 0.882 0.120 3 38551243 missense variant G/A snv 1.6E-05 7.0E-06 3
rs137854606 0.882 0.120 3 38604062 missense variant C/A snv 4
rs137854609 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 3
rs137854611 0.882 0.120 3 38597787 missense variant G/A;C;T snv 4.0E-06 3
rs137854612 0.851 0.120 3 38560170 missense variant C/T snv 4
rs137854615 0.851 0.120 3 38550989 missense variant A/G snv 4
rs137854616 1.000 0.080 3 38566465 missense variant C/T snv 2.8E-05 7.0E-06 1
rs137854617 0.882 0.120 3 38581002 stop gained C/A;T snv 1.1E-04 1.5E-04 3
rs137854618 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs137854620 1.000 0.080 3 38557268 stop gained C/T snv 1
rs1553605932 1.000 0.080 3 38622414 stop gained C/T snv 1
rs1559727990 1.000 0.080 3 38555727 stop gained G/A snv 1
rs1559729142 1.000 0.080 3 38556566 missense variant G/A snv 1
rs185492581 1.000 0.080 3 38630327 stop gained T/A;C snv 7.0E-06 1
rs185638763 0.882 0.120 3 38599001 missense variant G/A;T snv 1.2E-05 4
rs193922726 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 1
rs199473045 0.925 0.120 3 38633228 missense variant C/A;T snv 8.0E-06; 2.5E-04 2
rs199473050 1.000 0.080 3 38633098 missense variant A/C snv 4.4E-05 1.4E-05 1
rs199473051 0.925 0.120 3 38633058 missense variant C/T snv 2