Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3212948 0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53