Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs9394309 0.851 0.040 6 35654004 intron variant G/A snv 0.74 4
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs17662626 0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82