Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
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
rs2235749 0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs1042114 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1126671 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs2234918 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs678849 0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs1042363 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4