Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs1885884 13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs9316235 13 46871568 intron variant G/A snv 0.19 2