Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16