Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs2251219 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs28364997 0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs7597593 0.827 0.160 2 184668853 intron variant T/C snv 0.53 6