Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7956547 | 0.925 | 0.120 | 12 | 102465038 | intron variant | T/C | snv | 0.25 | 2 | ||
rs978458 | 0.925 | 0.120 | 12 | 102408461 | intron variant | T/C | snv | 0.69 | 2 | ||
rs121912430 | 1.000 | 0.120 | 12 | 102419637 | missense variant | C/T | snv | 1 | |||
rs5742617 | 12 | 102476127 | intron variant | C/T | snv | 8.7E-03 | 1 | ||||
rs5742629 | 1.000 | 0.040 | 12 | 102463485 | non coding transcript exon variant | T/C | snv | 0.32 | 1 | ||
rs5742643 | 12 | 102444085 | intron variant | T/C | snv | 0.76 | 1 | ||||
rs5742663 | 12 | 102430212 | intron variant | T/A;G | snv | 1 | |||||
rs5742683 | 12 | 102419939 | intron variant | A/G | snv | 3.3E-02 | 1 | ||||
rs587779350 | 1.000 | 0.120 | 12 | 102419619 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs7300373 | 12 | 102438008 | intron variant | T/G | snv | 1.4E-02 | 1 | ||||
rs9308315 | 12 | 102410115 | intron variant | A/C;T | snv | 1 |