Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs2454206 0.851 0.160 4 105275794 missense variant A/G;T snv 0.30; 6.4E-06 6