Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1052480459 | 0.925 | 0.160 | 15 | 48437837 | stop gained | C/A;G | snv | 7.0E-06 | 2 | ||
rs1057518881 | 0.827 | 0.200 | 15 | 48513656 | missense variant | C/A;G;T | snv | 6 | |||
rs1057521102 | 0.925 | 0.160 | 15 | 48510088 | missense variant | C/A;T | snv | 2 | |||
rs1057523406 | 0.925 | 0.160 | 15 | 48494209 | missense variant | C/A;G;T | snv | 2 | |||
rs1057524458 | 0.925 | 0.160 | 15 | 48489988 | missense variant | C/G | snv | 2 | |||
rs1060501017 | 0.925 | 0.160 | 15 | 48505136 | missense variant | A/C;G | snv | 2 | |||
rs1060501021 | 0.925 | 0.160 | 15 | 48494210 | missense variant | A/G | snv | 2 | |||
rs1060501022 | 0.925 | 0.160 | 15 | 48496214 | missense variant | A/G | snv | 2 | |||
rs1060501023 | 0.925 | 0.160 | 15 | 48430758 | stop gained | G/A | snv | 2 | |||
rs1060501029 | 0.925 | 0.160 | 15 | 48446909 | intron variant | T/C | snv | 2 | |||
rs1060501033 | 0.925 | 0.160 | 15 | 48411045 | frameshift variant | A/- | del | 2 | |||
rs1060501036 | 0.925 | 0.160 | 15 | 48513599 | missense variant | C/A;G | snv | 2 | |||
rs1060501055 | 0.925 | 0.160 | 15 | 48421997 | missense variant | A/C | snv | 2 | |||
rs1060501060 | 0.925 | 0.160 | 15 | 48425401 | frameshift variant | T/- | del | 2 | |||
rs1060501067 | 0.925 | 0.160 | 15 | 48415705 | frameshift variant | -/C | delins | 2 | |||
rs1060501073 | 0.925 | 0.160 | 15 | 48513612 | missense variant | C/A | snv | 2 | |||
rs1060501078 | 0.925 | 0.160 | 15 | 48505070 | missense variant | A/G;T | snv | 2 | |||
rs1060501082 | 0.925 | 0.160 | 15 | 48503811 | stop gained | G/A | snv | 2 | |||
rs1060501087 | 0.925 | 0.160 | 15 | 48446774 | missense variant | T/C | snv | 2 | |||
rs1060501093 | 0.925 | 0.160 | 15 | 48425491 | missense variant | T/C | snv | 2 | |||
rs1064793636 | 0.925 | 0.160 | 15 | 48497290 | frameshift variant | C/- | delins | 2 | |||
rs1064793637 | 0.925 | 0.160 | 15 | 48526201 | frameshift variant | T/- | delins | 2 | |||
rs1064793980 | 0.925 | 0.160 | 15 | 48434593 | splice donor variant | C/G;T | snv | 2 | |||
rs1064794282 | 0.925 | 0.160 | 15 | 48497316 | missense variant | C/T | snv | 2 | |||
rs1085307531 | 0.925 | 0.160 | 15 | 48444585 | missense variant | C/T | snv | 2 |