Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1553920379 | 0.776 | 0.160 | 4 | 101032294 | frameshift variant | -/AGTA | delins | 27 | |||
rs142110773 | 0.882 | 0.160 | 7 | 50463317 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 13 | |
rs886041095 | 0.827 | 0.160 | 12 | 13571930 | missense variant | C/T | snv | 11 | |||
rs869312702 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 10 | |||
rs869312704 | 0.882 | 0.160 | 2 | 161423752 | frameshift variant | -/GGCTGCA | delins | 10 | |||
rs1131691299 | 0.882 | 0.160 | X | 41341587 | frameshift variant | C/- | del | 9 | |||
rs886041097 | 0.882 | 0.160 | 4 | 139386152 | stop gained | C/G | snv | 9 | |||
rs863225082 | 0.827 | 0.160 | 6 | 43007265 | missense variant | G/A | snv | 7 | |||
rs1060499626 | 0.882 | 0.160 | 10 | 180034 | stop gained | C/T | snv | 6 | |||
rs1135402760 | 0.851 | 0.160 | 11 | 1451405 | frameshift variant | AG/- | delins | 6 | |||
rs1554297905 | 0.882 | 0.160 | 7 | 39686740 | missense variant | G/A | snv | 6 | |||
rs869312671 | 0.882 | 0.160 | 1 | 11144735 | missense variant | C/T | snv | 5 | |||
rs869312689 | 0.925 | 0.160 | 1 | 244053934 | missense variant | T/C | snv | 5 | |||
rs869312696 | 0.882 | 0.160 | 18 | 33739086 | stop gained | C/A | snv | 5 | |||
rs869312698 | 0.925 | 0.160 | 5 | 88804785 | missense variant | C/T | snv | 5 | |||
rs878853164 | 1.000 | 0.160 | 11 | 68157849 | stop gained | C/A | snv | 4.0E-06 | 5 | ||
rs1085307451 | 0.925 | 0.160 | 3 | 47848246 | missense variant | C/T | snv | 4 | |||
rs1555013332 | 0.882 | 0.160 | 11 | 70661635 | frameshift variant | -/T | delins | 4 | |||
rs1555447569 | 0.851 | 0.160 | 15 | 76471314 | frameshift variant | ATTG/- | delins | 4 | |||
rs534517447 | 0.925 | 0.160 | 11 | 120956935 | missense variant | G/A | snv | 2.9E-05 | 7.0E-06 | 4 | |
rs794726710 | 0.882 | 0.160 | 2 | 166013812 | stop gained | G/A | snv | 4 | |||
rs869312664 | 0.925 | 0.160 | 2 | 165386920 | stop gained | G/A;T | snv | 4 | |||
rs869312666 | 0.925 | 0.160 | 1 | 11129789 | missense variant | A/C | snv | 4 | |||
rs869312677 | 0.925 | 0.160 | 6 | 33446780 | frameshift variant | TTGGCAG/- | del | 4 | |||
rs869312699 | 0.925 | 0.160 | 11 | 120986102 | protein altering variant | CTGGCGCAGGAGGCC/GCT | delins | 4 |