| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs776095655 | 0.827 | 0.160 | 1 | 42927684 | missense variant | C/A;T | snv | 4.0E-06 | 8 | ||
| rs80359818 | 0.776 | 0.360 | 1 | 42930766 | missense variant | G/A | snv | 8 | |||
| rs80359826 | 0.807 | 0.120 | 1 | 42929018 | stop gained | G/A;T | snv | 4.0E-06 | 7 | ||
| rs13306758 | 0.807 | 0.360 | 1 | 42927148 | missense variant | G/A;T | snv | 2.8E-03 | 6 | ||
| rs1553155986 | 0.827 | 0.280 | 1 | 42929008 | missense variant | C/T | snv | 6 | |||
| rs796053248 | 0.807 | 0.360 | 1 | 42929885 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs202060209 | 0.925 | 0.040 | 1 | 42931047 | missense variant | G/A;T | snv | 2.4E-05 | 3 | ||
| rs387907312 | 0.882 | 0.200 | 1 | 42929918 | missense variant | G/A | snv | 3 | |||
| rs80359816 | 0.882 | 0.080 | 1 | 42930765 | missense variant | C/A;T | snv | 3 | |||
| rs121909739 | 0.925 | 0.040 | 1 | 42929242 | missense variant | C/T | snv | 2 | |||
| rs267607059 | 0.925 | 0.080 | 1 | 42927118 | missense variant | G/A | snv | 2 | |||
| rs267607061 | 0.925 | 0.040 | 1 | 42930865 | missense variant | G/A;T | snv | 7.0E-06 | 2 | ||
| rs796053253 | 0.925 | 0.040 | 1 | 42929211 | missense variant | G/A | snv | 2 | |||
| rs1553155887 | 1.000 | 1 | 42927704 | frameshift variant | T/- | delins | 1 | ||||
| rs1553156051 | 1.000 | 1 | 42929625 | stop gained | G/A | snv | 1 | ||||
| rs1553156199 | 1.000 | 1 | 42931093 | frameshift variant | -/C | delins | 1 | ||||
| rs1557646893 | 1.000 | 1 | 42931205 | splice acceptor variant | -/CC | delins | 1 | ||||
| rs796053263 | 1.000 | 1 | 42927685 | missense variant | G/A | snv | 1 | ||||
| rs869312673 | 1.000 | 1 | 42930036 | splice acceptor variant | C/G;T | snv | 1 |