Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs104893736 0.827 0.040 3 186539566 missense variant C/A snv 5
rs8027411 0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs104893685 0.882 0.040 3 133450432 missense variant C/A;T snv 4.0E-06; 2.0E-05 3
rs118203966 0.882 0.040 20 33851064 missense variant G/A snv 3
rs121909595 0.925 0.040 2 208124321 missense variant G/A snv 3
rs121909596 0.925 0.040 2 208124188 missense variant C/T snv 3
rs121909598 0.882 0.040 2 208121728 stop gained C/T snv 4.0E-06 3
rs121912973 0.882 0.040 21 43172105 missense variant G/A snv 3
rs17175798 0.925 0.040 15 79171618 intron variant C/A;T snv 3
rs398122392 0.882 0.040 2 208128258 stop gained C/A;G;T snv 2.4E-05; 8.0E-06 3
rs398122937 0.882 0.040 13 20142862 missense variant C/T snv 3
rs398122947 0.882 0.040 21 43170619 missense variant G/A snv 3
rs534473091 0.882 0.040 11 111908925 missense variant G/A snv 2.0E-05 4.9E-05 3
rs587783070 0.925 0.040 1 220143109 missense variant C/T snv 3
rs644242 0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 3
rs74315441 0.882 0.040 21 43169244 missense variant C/T snv 8.0E-06 3
rs781902168 0.882 0.040 11 111911694 missense variant G/A;C snv 3.2E-05 3
rs118203965 0.925 0.040 20 33850969 missense variant A/T snv 2
rs1215029143 1.000 0.040 X 154558608 missense variant G/A;T snv 2
rs121917867
MIP
0.925 0.040 12 56453703 missense variant G/A;C snv 4.0E-05 2
rs1227057051 1.000 0.040 21 43172266 missense variant G/A snv 8.2E-06 2
rs1250875000 0.925 0.040 21 6560927 missense variant C/A;T snv 2
rs140372256 0.925 0.040 2 208160859 stop gained C/A;G;T snv 1.5E-04; 1.6E-05; 4.0E-06 2