Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3742330 | 0.662 | 0.640 | 14 | 95087025 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 24 | ||
rs3135932 | 0.677 | 0.480 | 11 | 117993348 | missense variant | A/G | snv | 0.13 | 0.11 | 23 | |
rs5743810 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 21 | |
rs3819024 | 0.701 | 0.560 | 6 | 52185988 | upstream gene variant | A/G | snv | 0.34 | 17 | ||
rs181206 | 0.742 | 0.440 | 16 | 28502082 | missense variant | A/G | snv | 0.28 | 0.24 | 16 | |
rs4804803 | 0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 | 15 | ||
rs4135385 | 0.742 | 0.320 | 3 | 41237949 | non coding transcript exon variant | A/G | snv | 0.19 | 14 | ||
rs1131498 | 0.732 | 0.360 | 1 | 169707345 | missense variant | A/G | snv | 0.21 | 0.22 | 13 | |
rs2060793 | 0.776 | 0.240 | 11 | 14893764 | upstream gene variant | A/G | snv | 0.63 | 11 | ||
rs3764880 | 0.752 | 0.320 | X | 12906707 | start lost | A/G | snv | 0.31 | 0.30 | 11 | |
rs3811047 | 0.807 | 0.400 | 2 | 112913833 | missense variant | A/G | snv | 0.71 | 0.60 | 10 | |
rs3093662 | 0.851 | 0.200 | 6 | 31576412 | intron variant | A/G | snv | 7.1E-02 | 9 | ||
rs1061624 | 0.776 | 0.320 | 1 | 12207208 | 3 prime UTR variant | A/G | snv | 0.48 | 8 | ||
rs4851527 | 0.790 | 0.160 | 2 | 102005914 | intron variant | A/G | snv | 0.63 | 7 | ||
rs754342091 | 0.790 | 0.200 | 9 | 117712421 | missense variant | A/G | snv | 3.2E-05 | 1.4E-05 | 7 | |
rs10421768 | 0.807 | 0.120 | 19 | 35281996 | intron variant | A/G | snv | 0.21 | 6 | ||
rs2234711 | 0.827 | 0.080 | 6 | 137219383 | 5 prime UTR variant | A/G | snv | 0.43 | 6 | ||
rs3917225 | 0.807 | 0.160 | 2 | 102152842 | intron variant | A/G | snv | 0.36 | 6 | ||
rs735239 | 0.851 | 0.240 | 19 | 7748382 | upstream gene variant | A/G | snv | 0.26 | 5 | ||
rs4842407 | 0.882 | 0.200 | 12 | 78807293 | intron variant | A/G | snv | 0.35 | 4 | ||
rs2280789 | 0.925 | 0.080 | 17 | 35879999 | intron variant | A/G | snv | 0.16 | 3 | ||
rs5743604 | 0.925 | 0.040 | 4 | 38799664 | intron variant | A/G | snv | 0.36 | 3 | ||
rs76600635 | 0.925 | 0.040 | 4 | 38798702 | missense variant | A/G | snv | 8.2E-03 | 2.8E-03 | 3 | |
rs8105767 | 0.882 | 0.120 | 19 | 22032639 | non coding transcript exon variant | A/G | snv | 0.35 | 3 | ||
rs1135791 | 0.925 | 0.080 | 2 | 230177560 | missense variant | A/G | snv | 0.42 | 0.40 | 2 |