Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 38 | ||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs1475170339 | 0.732 | 0.240 | 16 | 1792325 | missense variant | T/C;G | snv | 18 | |||
rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
rs242557 | 0.752 | 0.200 | 17 | 45942346 | intron variant | G/A | snv | 0.36 | 12 | ||
rs6687758 | 0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 | 11 | ||
rs76980269 | 0.763 | 0.280 | 12 | 117330794 | synonymous variant | G/A | snv | 2.8E-05 | 4.2E-05 | 10 | |
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 9 | |||
rs63749855 | 0.790 | 0.200 | 17 | 46014271 | missense variant | T/G | snv | 8 | |||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 7 | ||
rs72824905 | 0.827 | 0.200 | 16 | 81908423 | missense variant | C/G;T | snv | 5.2E-03 | 6 | ||
rs7224296 | 0.882 | 0.160 | 17 | 46722680 | intron variant | G/A | snv | 0.59 | 5 | ||
rs762046989 | 0.851 | 0.200 | 17 | 45971867 | missense variant | C/G | snv | 8.0E-06 | 5 | ||
rs886039227 | 0.925 | 0.200 | 2 | 74378123 | missense variant | A/C | snv | 4 | |||
rs1768208 | 0.851 | 0.200 | 3 | 39481512 | intron variant | T/C | snv | 0.76 | 4 | ||
rs2471738 | 0.882 | 0.160 | 17 | 45998697 | intron variant | C/T | snv | 0.18 | 4 | ||
rs4239633 | 0.851 | 0.240 | 19 | 17631660 | intron variant | C/T | snv | 0.32 | 4 | ||
rs13302855 | 0.882 | 0.200 | 9 | 27595997 | intergenic variant | C/T | snv | 7.5E-02 | 3 | ||
rs1026683055 | 0.882 | 0.200 | 17 | 44351429 | missense variant | C/T | snv | 1.6E-05 | 1.5E-05 | 3 | |
rs1816 | 0.882 | 0.200 | 17 | 46199252 | intron variant | A/G | snv | 0.14 | 3 | ||
rs63751391 | 0.882 | 0.120 | 17 | 46010395 | missense variant | G/T | snv | 3 |