Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906309 0.925 0.160 15 72346579 frameshift variant -/GATA delins 4.0E-06; 8.0E-04 4.5E-04 10
rs121907966 0.882 0.160 15 72345477 missense variant G/A snv 4.0E-06 1.4E-05 9
rs1057519464 0.925 0.160 15 72347711 missense variant T/C;G snv 4.0E-06 7
rs1057519465 0.925 0.160 15 72346598 stop gained C/T snv 4.0E-06 7
rs1057519466 0.925 0.160 15 72346307 frameshift variant G/- del 7
rs121907978 0.925 0.160 15 72346296 missense variant C/G;T snv 7
rs773446161 0.925 0.160 15 72356555 stop gained G/A snv 4.0E-06 7
rs1057519463 0.882 0.240 15 72349160 frameshift variant GAACTCAT/- delins 6
rs1057519468 0.925 0.160 15 72345518 stop gained C/T snv 4.0E-06 6
rs121907954 0.807 0.120 15 72350518 missense variant C/G;T snv 1.3E-04 6
rs121907972 0.925 0.160 15 72353130 missense variant G/A snv 8.0E-06 1.4E-05 6
rs786204585 0.925 0.160 15 72344139 stop gained G/A snv 7.0E-06 6
rs1057519467 0.925 0.160 15 72345540 missense variant C/T snv 5
rs121907953 0.851 0.160 15 72353106 missense variant G/A snv 2.0E-05 5
rs370266293 0.925 0.160 15 72346679 missense variant C/G;T snv 1.0E-04 5
rs748190164 0.925 0.160 15 72356531 missense variant C/G;T snv 4.0E-06 4
rs762374961 0.925 0.160 15 72346235 stop gained C/A;T snv 4
rs121907960 1.000 0.120 15 72349148 inframe deletion GAA/- delins 3
rs121907971 0.882 0.120 15 72350551 missense variant C/G snv 4.0E-06 7.0E-06 3
rs121907981 0.882 0.120 15 72345550 missense variant C/G snv 1.2E-05 7.0E-06 3
rs267606862 0.882 0.160 15 72346681 stop gained C/T snv 3
rs587779406 1.000 0.120 15 72346552 synonymous variant G/A snv 8.0E-05 1.0E-04 3
rs755973971 0.882 0.120 15 72346661 missense variant T/A;C;G snv 7.6E-05; 1.6E-05 3
rs121907955 0.925 0.120 15 72345461 missense variant C/A;T snv 4.0E-06 2
rs121907956 0.925 0.120 15 72345476 missense variant C/T snv 5.6E-05 3.5E-05 2