| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12885713 | 0.827 | 0.200 | 14 | 90397013 | intron variant | C/A;G;T | snv | 5 | |||
| rs7135617 | 0.827 | 0.240 | 12 | 121631099 | intron variant | T/C;G | snv | 5 | |||
| rs7958311 | 0.851 | 0.160 | 12 | 121167552 | missense variant | G/A;C | snv | 0.25; 4.0E-06 | 5 | ||
| rs904571820 | 0.851 | 0.160 | 6 | 151842664 | start lost | A/G | snv | 4.0E-06 | 5 | ||
| rs1126464 | 1.000 | 0.040 | 16 | 89637957 | missense variant | G/A;C | snv | 1.3E-05; 0.26 | 4 | ||
| rs12982744 | 0.925 | 0.040 | 19 | 2177194 | intron variant | C/A;G;T | snv | 4 | |||
| rs1799986 | 0.851 | 0.120 | 12 | 57141483 | missense variant | C/A;T | snv | 8.0E-06; 0.13 | 4 | ||
| rs1940475 | 1.000 | 0.040 | 11 | 102722517 | missense variant | T/C;G | snv | 0.54 | 4 | ||
| rs2057768 | 0.925 | 0.120 | 16 | 27310774 | upstream gene variant | C/A;G;T | snv | 4 | |||
| rs2820436 | 0.882 | 0.040 | 1 | 219467338 | intergenic variant | A/C;G | snv | 4 | |||
| rs2908004 | 1.000 | 0.040 | 7 | 121329715 | missense variant | G/A;T | snv | 0.44; 4.0E-06 | 4 | ||
| rs8904 | 0.925 | 0.120 | 14 | 35402011 | 3 prime UTR variant | G/A;C;T | snv | 0.39; 4.0E-06 | 4 | ||
| rs11718863 | 0.882 | 0.080 | 3 | 15175196 | non coding transcript exon variant | A/G;T | snv | 0.21 | 3 | ||
| rs1871054 | 0.925 | 0.040 | 10 | 126093840 | intron variant | C/A;T | snv | 3 | |||
| rs2622873 | 0.882 | 0.040 | 1 | 103000497 | intron variant | T/C;G | snv | 3 | |||
| rs28936368 | 0.882 | 0.080 | 19 | 18783129 | missense variant | G/A;T | snv | 8.6E-04 | 3 | ||
| rs3740199 | 0.882 | 0.120 | 10 | 126330456 | missense variant | C/A;G | snv | 2.1E-03; 0.56 | 3 | ||
| rs3830675 | 1.000 | 0.040 | 10 | 87931195 | intron variant | -/TCTTA | delins | 3 | |||
| rs763098832 | 0.882 | 0.120 | 19 | 18783189 | missense variant | G/C;T | snv | 4.1E-06 | 3 | ||
| rs867986409 | 0.882 | 0.120 | 19 | 18784246 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
| rs10654220 | 1.000 | 0.040 | 12 | 123218875 | intron variant | -/TGT;TGTTGT | delins | 2 | |||
| rs1278279 | 0.925 | 0.040 | 10 | 126064909 | missense variant | G/A;C | snv | 0.27 | 2 | ||
| rs1905786 | 1.000 | 0.040 | 8 | 118939453 | intron variant | T/A;C | snv | 2 | |||
| rs4072286 | 1.000 | 0.040 | 8 | 141726333 | regulatory region variant | G/A;T | snv | 2 | |||
| rs4144782 | 0.925 | 0.040 | 2 | 118844296 | non coding transcript exon variant | A/C;G | snv | 2 |