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 | |||
rs1057518912 | 1.000 | 0.160 | 15 | 48456643 | frameshift variant | A/- | delins | 1 | |||
rs1057519320 | 0.807 | 0.160 | 15 | 48444574 | missense variant | G/A | snv | 7 | |||
rs1057519502 | 1.000 | 0.160 | 15 | 48495237 | stop gained | G/A | snv | 1 | |||
rs1057520131 | 0.925 | 0.240 | 15 | 48508633 | missense variant | A/C | snv | 2 | |||
rs1057520617 | 1.000 | 0.160 | 15 | 48430770 | missense variant | A/G | snv | 1 | |||
rs1057520728 | 1.000 | 0.160 | 15 | 48422057 | missense variant | A/C;G | snv | 1 | |||
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 | |||
rs1060501013 | 1.000 | 0.160 | 15 | 48488410 | frameshift variant | C/- | del | 1 | |||
rs1060501014 | 1.000 | 0.160 | 15 | 48415567 | missense variant | A/G | snv | 1 | |||
rs1060501016 | 1.000 | 0.160 | 15 | 48428395 | stop gained | A/T | snv | 1 | |||
rs1060501017 | 0.925 | 0.160 | 15 | 48505136 | missense variant | A/C;G | snv | 2 | |||
rs1060501019 | 1.000 | 0.160 | 15 | 48534131 | missense variant | A/C | snv | 1 | |||
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 | |||
rs1060501024 | 1.000 | 0.160 | 15 | 48503820 | stop gained | C/A | snv | 1 | |||
rs1060501026 | 1.000 | 0.160 | 15 | 48474299 | missense variant | C/G | snv | 1 | |||
rs1060501027 | 1.000 | 0.160 | 15 | 48503871 | frameshift variant | -/T | ins | 1 | |||
rs1060501029 | 0.925 | 0.160 | 15 | 48446909 | intron variant | T/C | snv | 2 | |||
rs1060501031 | 1.000 | 0.160 | 15 | 48463212 | frameshift variant | G/- | del | 1 | |||
rs1060501033 | 0.925 | 0.160 | 15 | 48411045 | frameshift variant | A/- | del | 2 |