Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
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
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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35