Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554266 1.000 0.040 20 58903791 splice region variant C/G;T snv 4.0E-06; 2.3E-03 4
rs1407040 20 58897119 intron variant C/T snv 0.70 4
rs6026578 20 58888417 5 prime UTR variant C/G snv 0.60 4