Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 3
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 3
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 6
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 22
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs397514495 0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 4
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 9
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 1
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14