Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37