Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs3132581 0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs2799573 0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs2721800 0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs2252865 0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs2021722 0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs17662626 0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs1715 0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5