Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 1 | ||
rs1799990 | 0.683 | 0.440 | 20 | 4699605 | missense variant | A/G | snv | 0.31 | 0.33 | 2 | |
rs1990622 | 0.742 | 0.200 | 7 | 12244161 | downstream gene variant | A/G | snv | 0.52 | 1 | ||
rs1980493 | 0.776 | 0.400 | 6 | 32395438 | intron variant | T/C | snv | 0.13 | 6 | ||
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 8 | ||
rs9268856 | 0.807 | 0.240 | 6 | 32461942 | intron variant | C/A;T | snv | 4 | |||
rs9268877 | 0.827 | 0.200 | 6 | 32463370 | intron variant | A/G;T | snv | 4 | |||
rs2814707 | 0.882 | 0.120 | 9 | 27536399 | non coding transcript exon variant | C/G;T | snv | 2 | |||
rs769446 | 0.882 | 0.120 | 19 | 44905371 | upstream gene variant | T/C | snv | 7.0E-02 | 1 | ||
rs302668 | 0.925 | 0.120 | 11 | 88143743 | intron variant | T/C | snv | 0.28 | 1 | ||
rs1358071 | 1.000 | 0.120 | 17 | 45725823 | intron variant | C/A;T | snv | 1 |