Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
rs55832599 | 0.716 | 0.360 | 17 | 7673821 | missense variant | G/A | snv | 18 | |||
rs1225976306 | 0.807 | 0.160 | 7 | 140924673 | missense variant | C/T | snv | 9.3E-06 | 8 | ||
rs866419664 | 0.882 | 0.040 | 17 | 7673821 | frameshift variant | -/TCCCA | delins | 5 | |||
rs878854600 | 0.851 | 0.240 | 22 | 23834262 | 3 prime UTR variant | C/T | snv | 4 | |||
rs387906812 | 0.882 | 0.320 | 22 | 23834152 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
rs74315513 | 0.925 | 0.160 | 22 | 23787203 | stop gained | C/T | snv | 2 | |||
rs55945045 | 1.000 | 0.040 | 6 | 149701841 | missense variant | G/A | snv | 3.6E-03; 4.0E-06 | 3.4E-03 | 1 | |
rs753300935 | 1.000 | 0.040 | 22 | 29661299 | missense variant | C/G;T | snv | 8.0E-06 | 7.0E-06 | 1 |