Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs10171367 2 233689021 intron variant C/A;G snv 3
rs10929301 2 233755003 splice region variant C/G;T snv 0.48 3
rs11673726 2 233755414 non coding transcript exon variant G/A;T snv 3
rs11680450 2 233688837 intron variant T/A;C snv 3
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs13002774 2 233685060 intron variant G/A;T snv 3
rs17862866 2 233702266 intron variant A/G;T snv 3
rs17864683 2 233670563 intron variant A/C;G snv 3
rs1875263 1.000 2 233716976 intron variant C/G;T snv 3
rs2417940 12 20864941 intron variant T/A;C snv 3
rs2602373 2 233653307 intron variant T/A;C snv 3
rs2741019 2 233602042 upstream gene variant C/A;G snv 3
rs2741028 2 233610268 intergenic variant G/A;T snv 3
rs2741042 2 233657271 intron variant C/A;T snv 3
rs3755319 0.925 0.120 2 233758936 intron variant A/C;G;T snv 3
rs4124874 0.851 0.120 2 233757013 intron variant T/A;G snv 3
rs4530361 2 233681395 intron variant A/G;T snv 3
rs7563561 2 233690345 intron variant T/C;G snv 3
rs7577677 2 233681970 synonymous variant C/A;G;T snv 0.35; 1.6E-05; 4.0E-06 3
rs7583278 2 233708761 intron variant C/A;G;T snv 3
rs7586110 2 233681881 intron variant T/A;G snv 3
rs7597496 2 233721797 non coding transcript exon variant A/C;G snv 3
rs10175828 2 233473171 downstream gene variant G/C;T snv 2
rs10203853 1.000 0.080 2 233778772 intron variant A/G;T snv 2