Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554386687 0.882 0.040 7 44242328 missense variant C/T snv 12
rs926027867 0.882 0.040 5 150251808 missense variant G/A;T snv 12
rs1287121256 0.882 0.040 5 150256777 missense variant C/G;T snv 7.0E-06 9
rs1554122526 0.882 0.040 5 150256811 missense variant A/G snv 9
rs1554121872 0.882 0.040 5 150250270 missense variant T/G snv 7
rs1554121875 0.882 0.040 5 150250281 missense variant T/C snv 7
rs1554123982 0.925 0.040 5 150273157 splice acceptor variant C/- delins 7
rs1554385305 0.925 0.040 7 44241784 splice acceptor variant C/T snv 7
rs1554122129 0.882 0.040 5 150252032 missense variant T/A snv 6
rs1057518961 0.925 0.040 14 102012450 missense variant C/T snv 5
rs1554122123 0.925 0.040 5 150251979 splice donor variant -/A delins 5
rs1057518940 0.925 0.040 19 38499718 missense variant G/A snv 4
rs1057518966 1.000 0.040 9 110800743 missense variant G/A snv 4
rs267606740 0.925 0.040 16 70481397 missense variant G/A snv 2.4E-05 1.4E-05 2
rs1048764460 1.000 0.040 16 70482809 stop gained C/A snv 5.6E-05 1
rs763944786 0.925 0.080 19 38469119 missense variant C/T snv 1.2E-05 1.4E-05 5
rs1566785990 0.851 0.120 14 77026534 missense variant A/G snv 12
rs61752992 0.807 0.120 X 154030621 splice acceptor variant TGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGC/- delins 9
rs756421370 0.807 0.120 1 29200513 splice donor variant -/A delins 1.4E-04 6.3E-05 8
rs267608463 0.925 0.120 X 154032206 splice donor variant C/A;T snv 5
rs751889864 0.925 0.120 9 110785664 missense variant T/A;C snv 4.0E-06; 1.6E-05 5
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs1555630216 0.790 0.160 18 10714931 splice acceptor variant C/T snv 22
rs1555648288 0.790 0.160 18 10795003 splice acceptor variant C/T snv 22
rs1554904159 0.851 0.160 11 1442607 splice donor variant G/A snv 11