Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057517384 1.000 0.160 13 51974830 frameshift variant -/GC delins 1
rs1057517444 1.000 0.160 13 51970692 frameshift variant TTTG/- delins 1
rs1057520235 1.000 0.160 13 51950277 missense variant A/G snv 1
rs1060499593 1.000 0.160 13 51970658 frameshift variant CACT/- del 1
rs1061472 0.925 0.200 13 51950352 missense variant T/C;G snv 0.54 2
rs1064797072 1.000 0.160 13 51944116 missense variant C/A snv 1
rs1085307057 1.000 0.160 13 51958517 stop gained G/A snv 1
rs1131691741 1.000 0.160 13 51937305 missense variant T/G snv 7.0E-06 1
rs1160679283 1.000 0.160 13 51935660 missense variant A/G snv 4.1E-06 1
rs1169959260 1.000 0.160 13 51949681 missense variant A/C snv 7.0E-06 1
rs1173050016 1.000 0.160 13 51964924 missense variant A/C snv 1
rs1173623580 1.000 0.160 13 51944143 missense variant G/A;C snv 4.0E-06; 8.0E-06 1
rs1176709391 1.000 0.160 13 51974069 frameshift variant TTGGGAG/- delins 1.2E-05 3.5E-05 1
rs1180133690 1.000 0.160 13 51958443 stop gained -/T delins 7.0E-06 1
rs1206016866 1.000 0.160 13 51944131 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1212479289 1.000 0.160 13 51960191 missense variant G/C;T snv 1
rs1213481140 1.000 0.160 13 51941201 missense variant C/T snv 8.0E-06 1
rs1217463955 1.000 0.160 13 51958340 missense variant G/C snv 4.0E-06 1
rs121907990 0.925 0.240 13 51937570 missense variant T/A;C snv 4.0E-06; 2.2E-04 2
rs121907992 1.000 0.160 13 51937583 missense variant C/T snv 2.8E-05 5.6E-05 1
rs121907993 1.000 0.160 13 51949772 missense variant G/A;C;T snv 6.0E-05; 2.8E-05; 4.0E-06 1
rs121907994 1.000 0.160 13 51950116 missense variant G/A snv 6.8E-05 1.4E-05 1
rs121907996 1.000 0.160 13 51946438 missense variant C/T snv 3.6E-05 5.6E-05 1
rs121907997 1.000 0.160 13 51958369 missense variant G/A;C snv 3.6E-05; 4.0E-06 1
rs121907998 1.000 0.160 13 51961849 missense variant A/C snv 5.2E-04 4.0E-04 1