Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894075 0.851 0.080 8 74362940 stop gained C/G snv 4.0E-06 2.1E-05 5
rs104894078 0.851 0.080 8 74360184 missense variant C/T snv 7.0E-06 5
rs864309503 0.882 0.200 22 30941503 missense variant G/A snv 5
rs121913597
MPZ
0.827 0.160 1 161307268 missense variant T/A snv 5
rs121913602
MPZ
0.851 0.120 1 161307308 missense variant T/A snv 5
rs281865128
MPZ
0.882 0.080 1 161306426 missense variant C/G;T snv 5
rs776757548 0.882 0.160 11 95847803 stop gained G/A;C snv 8.0E-06; 4.0E-06 5
rs119483085 0.851 0.160 8 133258374 stop gained G/A snv 7.0E-06 5
rs58332872 0.882 0.080 8 24956248 missense variant C/T snv 5
rs207482230
TFG
0.882 0.080 3 100748182 missense variant C/T snv 4.0E-06 5
rs267607143 0.851 0.080 12 109798823 missense variant G/A snv 7.0E-06 5
rs267607146 0.851 0.080 12 109800666 missense variant G/A;T snv 7.0E-06 5
rs281865137 0.851 0.080 10 62813496 missense variant C/T snv 4
rs397515442 0.882 0.080 8 74360194 missense variant A/G snv 4
rs1555937122 0.925 0.080 X 71223973 missense variant T/C snv 4
rs29001571 0.851 0.080 7 76303816 missense variant C/A;T snv 8.0E-06 4
rs121908160 0.882 0.080 1 10258602 missense variant A/T snv 4
rs57318642 0.851 0.200 1 156137203 missense variant C/T snv 1.4E-05 1.4E-05 4
rs59885338 0.851 0.120 1 156135268 missense variant C/T snv 3.6E-05 2.8E-05 4
rs145770066 0.882 0.080 19 49830790 missense variant C/T snv 3.8E-03 4.3E-03 4
rs572010627
MPZ
0.851 0.160 1 161306738 missense variant A/C;T snv 8.0E-06 4
rs199476138
ND3 ; COX3 ; ND4 ; ND4L ; ATP6
0.882 0.120 MT 9185 missense variant T/C snv 4
rs57105105 0.925 0.080 8 24953776 missense variant C/T snv 4
rs104894617 0.851 0.080 17 15260681 missense variant A/G snv 4
rs104894623 0.851 0.200 17 15239591 missense variant C/G;T snv 4