Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912893 | 0.708 | 0.400 | 12 | 47983721 | stop gained | G/A;T | snv | 15 | |||
rs121912874 | 0.716 | 0.400 | 12 | 47978329 | missense variant | G/A | snv | 14 | |||
rs794727261 | 0.716 | 0.400 | 12 | 47999953 | stop gained | G/T | snv | 14 | |||
rs121912879 | 0.925 | 0.080 | 12 | 47980017 | missense variant | C/G | snv | 2 | |||
rs1377808450 | 0.925 | 0.080 | 12 | 47980621 | missense variant | T/C | snv | 2 | |||
rs1289257741 | 0.925 | 0.080 | 17 | 80118690 | frameshift variant | AGGGA/- | del | 4.0E-06 | 2 | ||
rs121912878 | 1.000 | 0.080 | 12 | 47978389 | missense variant | C/T | snv | 1 | |||
rs121912888 | 1.000 | 0.080 | 12 | 47985946 | missense variant | C/T | snv | 1 | |||
rs121912899 | 1.000 | 0.080 | 12 | 47985771 | missense variant | C/A | snv | 1 | |||
rs1555165335 | 1.000 | 0.080 | 12 | 47978042 | inframe deletion | CACGGGGCCAGGAGGACC/- | delins | 1 | |||
rs1555166729 | 1.000 | 0.080 | 12 | 47983699 | missense variant | C/T | snv | 1 | |||
rs1555167156 | 1.000 | 0.080 | 12 | 47985956 | missense variant | C/T | snv | 1 | |||
rs1565681966 | 1.000 | 0.080 | 12 | 47985726 | splice donor variant | A/C | snv | 1 | |||
rs868417981 | 1.000 | 0.080 | 12 | 47986343 | missense variant | C/A;T | snv | 1 |