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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs945032 0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5