| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3737548 | 1.000 | 0.040 | 12 | 47997633 | synonymous variant | G/A;T | snv | 8.1E-06; 0.21 | 1 | ||
| rs1564861 | 1.000 | 0.040 | 8 | 118953670 | upstream gene variant | A/C | snv | 0.43 | 1 | ||
| rs1355782 | 1.000 | 0.040 | 3 | 131768822 | intron variant | T/C;G | snv | 1 | |||
| rs317630 | 1.000 | 0.040 | 12 | 69244067 | intron variant | T/C | snv | 0.76 | 1 | ||
| rs2171126 | 1.000 | 0.040 | 12 | 93773444 | intron variant | C/T | snv | 0.49 | 1 | ||
| rs945006 | 1.000 | 0.040 | 14 | 101562940 | 3 prime UTR variant | T/G | snv | 0.20 | 1 | ||
| rs4730250 | 1.000 | 0.040 | 7 | 107567250 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs61735963 | 1.000 | 0.040 | 1 | 1341803 | missense variant | C/A;T | snv | 2.9E-05; 1.5E-02 | 1 | ||
| rs11409738 | 1.000 | 0.040 | 7 | 96090522 | intron variant | A/-;AA;AAA;AAAA | delins | 1 | |||
| rs798726 | 1.000 | 0.040 | 4 | 1683484 | non coding transcript exon variant | T/C;G | snv | 1 | |||
| rs763810877 | 1.000 | 0.040 | 6 | 116806885 | missense variant | T/C | snv | 1.2E-04 | 3.5E-05 | 1 | |
| rs7810100 | 1.000 | 0.040 | 7 | 43176015 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs2856821 | 1.000 | 0.040 | 6 | 33078965 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs2287047 | 1.000 | 0.040 | 2 | 102157594 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs10172410 | 1.000 | 0.040 | 2 | 181487841 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs10795550 | 1.000 | 0.040 | 10 | 7562392 | 3 prime UTR variant | T/C;G | snv | 0.88 | 1 | ||
| rs10218792 | 1.000 | 0.040 | 1 | 245587630 | intron variant | T/G | snv | 0.26 | 1 | ||
| rs7941193 | 1.000 | 0.040 | 11 | 126500948 | intron variant | G/A;C | snv | 1 | |||
| rs6557013 | 1.000 | 0.040 | 5 | 97871838 | intron variant | T/A | snv | 0.97 | 1 | ||
| rs1998094 | 1.000 | 0.040 | 14 | 52116741 | intron variant | C/T | snv | 0.86 | 1 | ||
| rs11031191 | 1.000 | 0.040 | 11 | 30752733 | intergenic variant | G/C;T | snv | 0.27 | 1 | ||
| rs62435998 | 1.000 | 0.040 | 6 | 44727469 | upstream gene variant | C/T | snv | 0.28 | 1 | ||
| rs62435999 | 1.000 | 0.040 | 6 | 44727536 | upstream gene variant | T/G | snv | 0.28 | 1 | ||
| rs1404866 | 1.000 | 0.040 | 12 | 84970700 | intergenic variant | G/A;T | snv | 1 | |||
| rs2276455 | 1.000 | 0.040 | 12 | 47982354 | intron variant | G/A | snv | 0.38 | 1 |