Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs279826 1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs3798347 0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1885884 13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs9829896 3 20135980 intron variant C/A;T snv 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs11792633 0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs4722999 0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs678849 0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs12701020 0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800498 0.882 0.080 11 113420866 intron variant G/A snv 0.44 4