Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12720458 0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 20
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs1805128 0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs12720459 0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs267607277 0.807 0.120 14 90404386 missense variant A/G snv 6
rs398124647 0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs74315445 0.807 0.120 21 34449409 missense variant C/T snv 6.8E-05 5.3E-05 6
rs199473225 0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs199472910 0.827 0.120 7 150952508 missense variant G/A snv 1.2E-05 5
rs199472936 0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs151344631 0.827 0.200 11 2571333 missense variant G/A snv 8.0E-06 3.5E-05 5
rs121434500 0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 5
rs199473428 0.851 0.120 7 150951643 missense variant C/A;G;T snv 8.0E-06 4
rs120074186 0.851 0.120 11 2572979 stop gained G/A;C;T snv 1.6E-05; 4.0E-06; 4.0E-06 4
rs199472696 0.851 0.120 11 2570670 missense variant C/T snv 4.0E-06 1.4E-05 4
rs199472815 0.851 0.120 11 2778024 missense variant G/A;C snv 2.0E-05 4
rs397508118 0.851 0.120 11 2570720 frameshift variant GCGCT/- delins 1.4E-05 4
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs398124650 0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs199472944 0.882 0.120 7 150951552 missense variant G/A snv 3