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
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
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
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8