| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
| 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 | |||
| rs1940475 | 1.000 | 0.040 | 11 | 102722517 | missense variant | T/C;G | snv | 0.54 | 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 | ||
| rs1042667 | 1.000 | 0.040 | 17 | 72124410 | 3 prime UTR variant | A/C | snv | 0.41 | 0.36 | 3 | |
| rs10492367 | 0.882 | 0.040 | 12 | 27862037 | regulatory region variant | G/T | snv | 0.12 | 3 | ||
| rs10947262 | 0.925 | 0.040 | 6 | 32405535 | non coding transcript exon variant | C/T | snv | 0.12 | 3 | ||
| rs10948172 | 0.882 | 0.040 | 6 | 44809954 | intron variant | A/G | snv | 0.27 | 3 | ||
| rs12901499 | 0.882 | 0.040 | 15 | 67078107 | intron variant | G/A | snv | 0.45 | 3 | ||
| rs1800802 | 0.925 | 0.040 | 12 | 14885985 | intron variant | A/G | snv | 0.15 | 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 | |||
| rs3830675 | 1.000 | 0.040 | 10 | 87931195 | intron variant | -/TCTTA | delins | 3 | |||
| rs532464664 | 0.882 | 0.040 | 22 | 41238083 | frameshift variant | -/GCCCGCGC | delins | 4.8E-03 | 1.2E-02 | 3 | |
| rs715572 | 0.925 | 0.040 | 22 | 32838944 | intron variant | G/A | snv | 0.18 | 3 | ||
| rs75621460 | 0.882 | 0.040 | 19 | 41327879 | intron variant | G/A | snv | 2.0E-02 | 3 | ||
| rs77245812 | 0.882 | 0.040 | 2 | 20003169 | missense variant | G/A | snv | 1.5E-02 | 1.2E-02 | 3 | |
| rs1044122 | 0.925 | 0.040 | 10 | 126036209 | synonymous variant | A/G | snv | 0.27 | 0.26 | 2 | |
| rs10654220 | 1.000 | 0.040 | 12 | 123218875 | intron variant | -/TGT;TGTTGT | delins | 2 | |||
| rs11564299 | 0.925 | 0.040 | 18 | 28180064 | upstream gene variant | A/G | snv | 0.17 | 2 | ||
| rs115740542 | 0.925 | 0.040 | 6 | 26123274 | intron variant | T/C | snv | 3.6E-02 | 2 | ||
| rs1278279 | 0.925 | 0.040 | 10 | 126064909 | missense variant | G/A;C | snv | 0.27 | 2 | ||
| rs13301537 | 0.925 | 0.040 | 9 | 92466765 | intron variant | A/G | snv | 0.38 | 2 |