Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 1
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs4633 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7