Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 34 | ||
rs11554290 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 25 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 22 | ||
rs121913255 | 0.667 | 0.400 | 1 | 114713907 | missense variant | T/A;G | snv | 19 | |||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 14 | ||
rs121913366 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 7 | |||
rs121913378 | 0.776 | 0.280 | 7 | 140753337 | missense variant | C/A;G;T | snv | 6 | |||
rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 3 | ||
rs121913254 | 0.658 | 0.440 | 1 | 114713909 | stop gained | G/A;C;T | snv | 3 | |||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 2 | |||
rs993022333 | 0.851 | 0.080 | 4 | 54733173 | missense variant | A/C;T | snv | 2 | |||
rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 1 | |||
rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 1 | |||
rs868224085 | 1.000 | 0.040 | 2 | 221482474 | missense variant | G/A | snv | 1 | |||
rs267601191 | 1.000 | 0.040 | 7 | 100819817 | missense variant | G/A | snv | 1 | |||
rs1451501407 | 1.000 | 0.040 | 17 | 8006628 | missense variant | G/A | snv | 1 | |||
rs1238066548 | 1.000 | 0.040 | 19 | 38595699 | missense variant | G/A;T | snv | 1 | |||
rs267601046 | 1.000 | 0.040 | 6 | 43283303 | missense variant | C/T | snv | 1 | |||
rs1057519695 | 0.641 | 0.520 | 1 | 114713907 | missense variant | TT/CA;CC | mnv | 1 | |||
rs1057519834 | 0.658 | 0.480 | 1 | 114713908 | missense variant | TG/CT | mnv | 1 | |||
rs907102077 | 1.000 | 0.040 | 3 | 9760752 | missense variant | G/A | snv | 1 | |||
rs1484691555 | 1.000 | 0.040 | 20 | 9539512 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1277219458 | 1.000 | 0.040 | 2 | 241143002 | missense variant | C/T | snv | 1 | |||
rs779173667 | 1.000 | 0.040 | 4 | 54290418 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs267605306 | 1.000 | 0.040 | 19 | 14446504 | missense variant | C/G;T | snv | 1.6E-05 | 1 |