Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs993226 | 0.851 | 0.160 | 12 | 84492794 | intergenic variant | T/G | snv | 6.3E-02 | 4 | ||
rs941934 | 0.851 | 0.200 | 1 | 152417976 | intron variant | T/A;C | snv | 5 | |||
rs9357733 | 0.851 | 0.160 | 6 | 52427338 | intron variant | A/G | snv | 0.19 | 4 | ||
rs7936562 | 0.882 | 0.160 | 11 | 76567214 | intergenic variant | T/C | snv | 0.59 | 4 | ||
rs7936323 | 0.882 | 0.160 | 11 | 76582714 | intergenic variant | G/A | snv | 0.44 | 6 | ||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 12 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs7534334 | 0.882 | 0.160 | 1 | 153205376 | downstream gene variant | C/T | snv | 0.25 | 3 | ||
rs7518129 | 0.882 | 0.120 | 1 | 173194429 | intron variant | A/G | snv | 0.47 | 3 | ||
rs73196739 | 0.925 | 0.120 | 3 | 188684683 | intron variant | C/T | snv | 0.13 | 2 | ||
rs731236 | 0.542 | 0.760 | 12 | 47844974 | synonymous variant | A/G | snv | 0.33 | 0.34 | 81 | |
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 14 | ||
rs7124842 | 0.882 | 0.160 | 11 | 76600576 | intergenic variant | G/A;C;T | snv | 3 | |||
rs712484 | 0.882 | 0.160 | 14 | 48081576 | intergenic variant | C/A | snv | 0.14 | 3 | ||
rs6894249 | 0.776 | 0.160 | 5 | 132461855 | non coding transcript exon variant | A/G | snv | 0.45 | 9 | ||
rs6693927 | 0.925 | 0.120 | 1 | 153071533 | upstream gene variant | G/A | snv | 0.35 | 2 | ||
rs6594499 | 0.882 | 0.120 | 5 | 111134439 | downstream gene variant | C/A | snv | 0.56 | 4 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs62623446 | 0.882 | 0.120 | 12 | 54974507 | missense variant | C/T | snv | 4.5E-02 | 4.4E-02 | 3 | |
rs61839660 | 0.776 | 0.280 | 10 | 6052734 | intron variant | C/T | snv | 5.7E-02 | 9 | ||
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs6010620 | 0.701 | 0.360 | 20 | 63678486 | intron variant | A/C;G | snv | 21 | |||
rs574456 | 0.882 | 0.160 | 2 | 140644133 | intron variant | A/T | snv | 8.1E-02 | 3 | ||
rs5744292 | 0.851 | 0.200 | 11 | 112143413 | 3 prime UTR variant | T/C | snv | 0.16 | 4 |