| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918392 | 0.925 | 0.040 | 19 | 44907777 | missense variant | G/A | snv | 3.6E-05 | 7.0E-06 | 2 | |
| rs121918399 | 0.925 | 0.120 | 19 | 44907843 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
| rs1335550286 | 1.000 | 0.040 | 19 | 44909005 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
| rs1466963971 | 0.925 | 0.120 | 19 | 44908640 | missense variant | T/G | snv | 4.5E-06 | 2 | ||
| rs201672011 | 1.000 | 0.080 | 19 | 44907807 | missense variant | G/A | snv | 1.2E-04 | 4.8E-04 | 2 | |
| rs449647 | 0.925 | 0.120 | 19 | 44905307 | upstream gene variant | A/T | snv | 0.21 | 2 | ||
| rs7259620 | 0.925 | 0.120 | 19 | 44904531 | upstream gene variant | G/A;C | snv | 2 | |||
| rs769452 | 0.925 | 0.160 | 19 | 44907853 | missense variant | T/C | snv | 2.5E-03 | 1.9E-03 | 2 | |
| rs1050106163 | 1.000 | 0.040 | 19 | 44908618 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1081105 | 1.000 | 0.080 | 19 | 44909698 | non coding transcript exon variant | A/C | snv | 3.0E-02 | 1 | ||
| rs115299243 | 19 | 44907291 | non coding transcript exon variant | A/G | snv | 7.1E-03 | 1 | ||||
| rs11542029 | 1.000 | 0.080 | 19 | 44907864 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 1.2E-05 | 1 | ||
| rs11542035 | 19 | 44908706 | missense variant | G/A | snv | 1.9E-05 | 2.8E-05 | 1 | |||
| rs11542037 | 1.000 | 0.080 | 19 | 44908657 | missense variant | C/A;T | snv | 5.2E-06 | 1 | ||
| rs1167428194 | 1.000 | 0.080 | 19 | 44908634 | missense variant | A/C | snv | 1 | |||
| rs121918395 | 19 | 44909032 | missense variant | C/A;T | snv | 6.9E-06; 4.2E-05 | 1 | ||||
| rs121918396 | 1.000 | 0.080 | 19 | 44908979 | stop gained | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
| rs121918398 | 19 | 44909171 | missense variant | G/A | snv | 4.5E-06 | 1 | ||||
| rs1270059098 | 1.000 | 0.080 | 19 | 44906634 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1275147925 | 1.000 | 0.080 | 19 | 44906613 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs1424027593 | 1.000 | 0.080 | 19 | 44908639 | missense variant | C/A | snv | 1 | |||
| rs142480126 | 19 | 44907825 | missense variant | G/A | snv | 8.0E-06 | 1 | ||||
| rs1438607869 | 1.000 | 0.080 | 19 | 44908741 | missense variant | G/A | snv | 1 | |||
| rs1440976751 | 1.000 | 0.080 | 19 | 44907789 | missense variant | G/A | snv | 1 | |||
| rs1458301734 | 1.000 | 0.080 | 19 | 44908687 | missense variant | G/A;T | snv | 5.9E-06 | 1 |