Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 39
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 17
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 17
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15