| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs405509 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 30 | ||
| rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
| rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 11 | ||
| rs769446 | 0.882 | 0.120 | 19 | 44905371 | upstream gene variant | T/C | snv | 7.0E-02 | 6 | ||
| rs769450 | 0.925 | 0.120 | 19 | 44907187 | non coding transcript exon variant | G/A | snv | 0.39 | 5 | ||
| rs1233347077 | 0.851 | 0.160 | 19 | 44905894 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
| rs1335550286 | 1.000 | 0.040 | 19 | 44909005 | missense variant | G/A | snv | 7.0E-06 | 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 | |||
| 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 | ||||
| rs1167428194 | 1.000 | 0.080 | 19 | 44908634 | missense variant | A/C | snv | 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 | |||
| 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 | |||
| rs200703101 | 19 | 44908757 | missense variant | G/C;T | snv | 1 | |||||
| rs397514253 | 1.000 | 0.080 | 19 | 44908531 | splice acceptor variant | A/G | snv | 1 | |||
| rs515726148 | 1.000 | 0.160 | 19 | 44908792 | inframe deletion | TCC/- | delins | 2.8E-05 | 1 | ||
| rs868094551 | 1.000 | 0.080 | 19 | 44908768 | missense variant | C/A;T | snv | 1 | |||
| rs981058595 | 1.000 | 0.080 | 19 | 44908847 | missense variant | C/A | snv | 1 | |||
| rs1270059098 | 1.000 | 0.080 | 19 | 44906634 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs777551553 | 1.000 | 0.080 | 19 | 44906639 | stop gained | G/A | snv | 4.0E-06 | 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 |