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 92
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs1859168 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13