Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
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
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
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
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
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
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
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33