Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35