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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
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
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs3213207 0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs75634836 0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs1326656542 0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs2271933 0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs1386483 0.790 0.080 12 72018714 intron variant T/C snv 0.53 9