Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764929617 0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs121918398 19 44909171 missense variant G/A snv 4.5E-06 1
rs1466963971 0.925 0.120 19 44908640 missense variant T/G snv 4.5E-06 2
rs11542037 1.000 0.080 19 44908657 missense variant C/A;T snv 5.2E-06 1
rs1458301734 1.000 0.080 19 44908687 missense variant G/A;T snv 5.9E-06 1
rs573658040 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs779569800 1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 1
rs387906567 0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs748703149 0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs267606664 0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 5
rs121918397 0.882 0.200 19 44908784 missense variant G/A;C snv 6.5E-06 3
rs121918394 0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs121918395 19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05 1
rs267606663 0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06 3
rs121918399 0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 2
rs142480126 19 44907825 missense variant G/A snv 8.0E-06 1
rs533904656 1.000 0.080 19 44907768 missense variant G/A;C snv 1.8E-04; 8.2E-06 1
rs267606661 0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs28931576 19 44907894 missense variant A/G snv 1.2E-05 1.4E-05 1
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs761592007 0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs121918396 1.000 0.080 19 44908979 stop gained G/A snv 1.6E-05 3.5E-05 1
rs11542035 19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs752600356 0.851 0.280 19 44908681 missense variant G/A;C snv 2.3E-05 1.4E-05 4
rs28931578 19 44908751 missense variant G/A;C;T snv 3.2E-05 1