Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386833981 0.925 0.120 13 77000517 missense variant T/G snv 3
rs104894385 0.925 0.120 13 76992176 stop gained G/A;T snv 2.7E-05; 3.1E-05 2
rs104894386 0.925 0.120 13 76995077 missense variant G/A;C snv 8.0E-06 2
rs1555274338 1.000 0.120 13 77000567 stop gained G/A;C snv 2
rs28940280 0.925 0.120 13 77000580 missense variant G/A snv 8.0E-06 2
rs386833975 0.925 0.120 13 76995990 missense variant A/G snv 2
rs386833980 0.925 0.120 13 76996086 stop gained G/A snv 1.6E-05 3.5E-05 2
rs546989392 0.925 0.120 13 76996010 stop gained C/T snv 2.0E-05 7.7E-05 2
rs121908292 1.000 0.120 13 77000799 stop gained G/T snv 1
rs147065248 1.000 0.120 13 76996034 missense variant T/C snv 1.2E-05 7.0E-06 1
rs148862100 1.000 0.120 13 77000866 missense variant A/G snv 1.3E-05 7.0E-06 1
rs1555274014 1.000 0.120 13 76996128 splice donor variant G/A snv 1
rs1566219136 1.000 0.120 13 76995993 missense variant G/A snv 1
rs200348035 1.000 0.120 13 76992182 stop gained G/A;T snv 4.5E-06 1
rs202146713 1.000 0.120 13 76995233 splice region variant G/C snv 1.2E-05 2.1E-05 1
rs267606738 1.000 0.120 13 76995119 missense variant G/A snv 1
rs386833963 1.000 0.120 13 77000771 stop gained C/A snv 1
rs386833968 1.000 0.120 13 77000882 stop gained G/A;T snv 4.3E-06 1
rs386833971 1.000 0.120 13 76995175 stop gained C/T snv 2.4E-05 1
rs386833972 1.000 0.120 13 76995939 stop gained T/G snv 4.0E-06; 4.0E-06 1
rs386833974 1.000 0.120 13 76995980 stop gained C/T snv 1
rs386833976 1.000 0.120 13 76996008 missense variant T/C snv 4.0E-06 1
rs386833977 1.000 0.120 13 76996028 missense variant C/T snv 1
rs386833978 1.000 0.120 13 76996035 missense variant G/C snv 1
rs730882146 1.000 0.120 13 77000680 missense variant G/A snv 4.0E-06 1