Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32