| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 7 | ||
| rs1269304342 | 1.000 | 0.040 | 10 | 98425560 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs6465657 | 0.807 | 0.280 | 7 | 98187015 | intron variant | C/T | snv | 0.41 | 0.37 | 7 | |
| rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
| rs781198499 | 1.000 | 0.040 | 5 | 96765321 | missense variant | T/A;C | snv | 7.1E-06 | 1 | ||
| rs1334613121 | 0.925 | 0.080 | 14 | 93787688 | missense variant | C/T | snv | 3 | |||
| rs10852628 | 1.000 | 0.040 | 16 | 90013519 | intron variant | C/A;T | snv | 1 | |||
| rs8059973 | 1.000 | 0.040 | 16 | 90013126 | intron variant | A/G | snv | 0.78 | 1 | ||
| rs11076650 | 1.000 | 0.040 | 16 | 90001533 | non coding transcript exon variant | G/A | snv | 0.49 | 1 | ||
| rs4785763 | 0.925 | 0.120 | 16 | 90000528 | non coding transcript exon variant | A/C;T | snv | 3 | |||
| rs4785759 | 1.000 | 0.040 | 16 | 89984472 | intron variant | A/C;G | snv | 1 | |||
| rs4238833 | 1.000 | 0.040 | 16 | 89984281 | intron variant | G/T | snv | 0.60 | 2 | ||
| rs1063045 | 1.000 | 0.040 | 8 | 89982791 | synonymous variant | C/T | snv | 0.35 | 0.33 | 1 | |
| rs11648898 | 1.000 | 0.040 | 16 | 89979578 | non coding transcript exon variant | A/G | snv | 0.17 | 1 | ||
| rs4408545 | 1.000 | 0.040 | 16 | 89977620 | non coding transcript exon variant | C/G;T | snv | 0.40 | 2 | ||
| rs34767364 | 0.701 | 0.280 | 8 | 89971232 | missense variant | G/A;C | snv | 2.5E-03 | 20 | ||
| rs4785752 | 1.000 | 0.040 | 16 | 89968733 | upstream gene variant | A/G | snv | 0.42 | 2 | ||
| rs4785751 | 1.000 | 0.040 | 16 | 89963009 | intron variant | G/A | snv | 0.37 | 1 | ||
| rs867185 | 1.000 | 0.040 | 8 | 89962922 | intron variant | G/A | snv | 0.51 | 1 | ||
| rs8051733 | 1.000 | 0.040 | 16 | 89957798 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs7195043 | 1.000 | 0.040 | 16 | 89954453 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs9995 | 1.000 | 0.040 | 8 | 89933828 | 3 prime UTR variant | A/G | snv | 0.32 | 1 | ||
| rs1805009 | 0.790 | 0.280 | 16 | 89920138 | missense variant | G/A;C | snv | 4.0E-06; 9.1E-03 | 9 | ||
| rs371055548 | 0.925 | 0.080 | 16 | 89919798 | synonymous variant | C/T | snv | 2.4E-05 | 2.1E-05 | 2 | |
| rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 |