Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
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
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 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
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40