Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057520719 | 1.000 | 0.120 | X | 154773227 | missense variant | G/A | snv | 1 | |||
rs1114167422 | 0.776 | 0.320 | X | 154773148 | missense variant | A/G | snv | 11 | |||
rs121912287 | 1.000 | 0.120 | X | 154765525 | missense variant | CT/TC | mnv | 1 | |||
rs121912288 | 0.925 | 0.120 | X | 154773152 | missense variant | C/T | snv | 2 | |||
rs121912289 | 0.925 | 0.120 | X | 154774672 | missense variant | C/T | snv | 2 | |||
rs121912290 | 0.925 | 0.120 | X | 154770792 | missense variant | C/G;T | snv | 2 | |||
rs121912291 | 0.925 | 0.120 | X | 154770808 | missense variant | G/A | snv | 2 | |||
rs121912292 | 0.925 | 0.120 | X | 154765478 | missense variant | C/G | snv | 2 | |||
rs121912293 | 0.925 | 0.120 | X | 154765465 | missense variant | T/G | snv | 2 | |||
rs121912294 | 1.000 | 0.120 | X | 154765949 | missense variant | CT/TA | mnv | 1 | |||
rs121912295 | 0.925 | 0.120 | X | 154774651 | missense variant | G/A | snv | 2 | |||
rs121912296 | 0.925 | 0.120 | X | 154765474 | missense variant | A/G | snv | 2 | |||
rs121912297 | 0.925 | 0.120 | X | 154765931 | missense variant | A/G | snv | 2 | |||
rs121912298 | 0.925 | 0.120 | X | 154773144 | missense variant | G/A | snv | 2 | |||
rs121912299 | 0.925 | 0.120 | X | 154774650 | missense variant | G/A | snv | 2 | |||
rs121912300 | 0.925 | 0.120 | X | 154773143 | missense variant | T/C | snv | 2 | |||
rs121912301 | 0.925 | 0.120 | X | 154765929 | missense variant | G/C | snv | 2 | |||
rs121912302 | 0.925 | 0.120 | X | 154765480 | missense variant | G/A | snv | 2 | |||
rs121912303 | 0.925 | 0.120 | X | 154762970 | missense variant | C/T | snv | 2 | |||
rs121912304 | 0.925 | 0.120 | X | 154765505 | missense variant | C/T | snv | 2 | |||
rs121912305 | 0.925 | 0.120 | X | 154766313 | missense variant | A/G | snv | 2 | |||
rs121912306 | 0.925 | 0.120 | X | 154765949 | missense variant | C/T | snv | 2 | |||
rs137854489 | 0.925 | 0.120 | X | 154765466 | inframe deletion | CTT/- | delins | 2 | |||
rs137854491 | 0.925 | 0.120 | X | 154765450 | missense variant | C/A;G | snv | 2 | |||
rs137854492 | 1.000 | 0.120 | X | 154773163 | missense variant | A/G | snv | 1 |