Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs2070150 0.827 0.280 1 161791486 missense variant G/C snv 0.14 9.2E-02 6
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1993116 0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs13078 0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24