| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs864309499 | 0.827 | 0.240 | 22 | 41526319 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
| rs375761361 | 0.827 | 0.240 | 22 | 41527949 | missense variant | C/G;T | snv | 4.0E-06; 3.6E-05 | 9 | ||
| rs117078955 | 1.000 | 0.080 | 22 | 41501983 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
| rs141772938 | 1.000 | 22 | 41507837 | missense variant | C/G | snv | 3.7E-03 | 3.8E-03 | 1 | ||
| rs150129663 | 22 | 41518528 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 1 | |||
| rs727563 | 1.000 | 0.040 | 22 | 41471373 | intron variant | C/T | snv | 0.59 | 1 | ||
| rs786200924 | 1.000 | 22 | 41507953 | missense variant | C/G | snv | 1 | ||||
| rs786204828 | 1.000 | 22 | 41515858 | missense variant | G/A | snv | 1 | ||||
| rs9611602 | 22 | 41512401 | intron variant | T/C | snv | 0.19 | 1 | ||||
| rs1114167284 | 1.000 | 22 | 41528607 | frameshift variant | CA/- | delins | 1 | ||||
| rs1555890974 | 22 | 41527919 | frameshift variant | AG/- | del | 1 | |||||
| rs786204830 | 1.000 | 22 | 41528595 | frameshift variant | GGAA/- | delins | 1 | ||||
| rs752034900 | 1.000 | 22 | 41527315 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
| rs786204829 | 1.000 | 22 | 41528022 | missense variant | G/C | snv | 1 |