Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519051 0.882 0.200 5 132390825 stop gained T/G snv 3
rs118203945 0.882 0.280 1 11273836 missense variant A/G snv 3
rs121908893 1.000 0.160 5 132385435 stop gained C/A;T snv 5.3E-04; 1.2E-04 3
rs768272475 0.925 0.240 1 179345018 synonymous variant A/G snv 4.0E-06 2
rs1022453298 1.000 0.160 5 132370023 frameshift variant C/- delins 1
rs1057516402 1.000 0.160 5 132394183 splice acceptor variant A/G snv 1
rs1057516765 1.000 0.160 5 132378475 stop gained C/G snv 1
rs1057516797 1.000 0.160 5 132370127 frameshift variant -/GACGCCG delins 1
rs1057516805 1.000 0.160 5 132387024 splice acceptor variant G/C snv 1
rs1057517069 1.000 0.160 5 132370366 splice donor variant G/A snv 1
rs1057517106 1.000 0.160 5 132378377 splice acceptor variant G/T snv 1
rs1057517306 1.000 0.160 5 132393678 frameshift variant -/C delins 1
rs1057518297 1.000 0.160 5 132390889 stop gained C/T snv 1
rs121908887 1.000 0.160 5 132390838 stop gained -/A delins 1
rs121908890 1.000 0.160 5 132384154 missense variant C/T snv 4.0E-06 1
rs121908892 1.000 0.160 5 132369975 start lost G/A;T snv 1
rs1253026669 1.000 0.160 5 132370224 stop gained C/G;T snv 1
rs1385634398 1.000 0.160 5 132390701 missense variant C/T snv 8.0E-06 1
rs1457258524 1.000 0.160 5 132385375 missense variant G/C snv 4.0E-06 1
rs150544263 1.000 0.160 5 132389012 missense variant T/A;C snv 4.0E-06; 5.2E-05 1
rs151231558 1.000 0.160 5 132378408 missense variant G/A;T snv 1.2E-05; 5.6E-05 1
rs1554085861 1.000 0.160 5 132369882 start lost GCCTGGTCGGCGGCGGGTGCCCCGCGCGCACGCGCAAAGCCCGCCGCGTTCCCCGACCCCAGGCCGCGCTCTGTGGGCCTCTGAGGGCGGCATGCGGGACTACGACGAGGTGA/- del 1
rs1554085885 1.000 0.160 5 132369974 start lost T/G snv 1
rs1554085892 1.000 0.160 5 132369985 frameshift variant G/- del 1
rs1554085942 1.000 0.160 5 132370157 stop gained G/A snv 1