| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1114167409 | 1.000 | 0.120 | 17 | 50201444 | inframe deletion | TTGGCC/- | delins | 1 | |||
| rs1114167412 | 1.000 | 0.120 | 7 | 94410492 | missense variant | G/C | snv | 1 | |||
| rs1131692320 | 1.000 | 0.120 | 17 | 50187103 | missense variant | C/T | snv | 1 | |||
| rs1554396283 | 1.000 | 0.120 | 7 | 94410926 | missense variant | G/T | snv | 1 | |||
| rs1800250 | 1.000 | 0.120 | 7 | 94427801 | missense variant | A/C | snv | 1 | |||
| rs267606742 | 1.000 | 0.120 | 7 | 94427628 | missense variant | G/A | snv | 1 | |||
| rs67609234 | 1.000 | 0.120 | 7 | 94425832 | missense variant | G/A;T | snv | 1 | |||
| rs67641695 | 1.000 | 0.120 | 17 | 50188592 | missense variant | C/T | snv | 1 | |||
| rs67729041 | 1.000 | 0.120 | 7 | 94409778 | missense variant | G/A;T | snv | 1 | |||
| rs72645320 | 1.000 | 0.120 | 17 | 50197053 | missense variant | C/T | snv | 1 | |||
| rs72645363 | 1.000 | 0.120 | 17 | 50195931 | missense variant | C/G | snv | 1 | |||
| rs72656320 | 1.000 | 0.120 | 17 | 50187095 | missense variant | C/T | snv | 1 | |||
| rs72656353 | 1.000 | 0.120 | 17 | 50185506 | missense variant | A/G | snv | 1 | |||
| rs72656402 | 1.000 | 0.120 | 7 | 94410429 | missense variant | G/T | snv | 1 | |||
| rs72658125 | 1.000 | 0.120 | 7 | 94413110 | missense variant | G/A | snv | 1 | |||
| rs72658126 | 1.000 | 0.120 | 7 | 94413128 | missense variant | G/C | snv | 1 | |||
| rs72658150 | 1.000 | 0.120 | 7 | 94417797 | missense variant | G/T | snv | 1 | |||
| rs72658186 | 1.000 | 0.120 | 7 | 94421045 | missense variant | G/A | snv | 1 | |||
| rs72658191 | 1.000 | 0.120 | 7 | 94423011 | missense variant | G/A | snv | 1 | |||
| rs72658200 | 1.000 | 0.120 | 7 | 94424345 | missense variant | G/A | snv | 1 | |||
| rs72659312 | 1.000 | 0.120 | 7 | 94425759 | missense variant | G/A | snv | 1 | |||
| rs72659316 | 1.000 | 0.120 | 7 | 94426026 | missense variant | G/T | snv | 1 | |||
| rs72659337 | 1.000 | 0.120 | 7 | 94427646 | missense variant | G/C | snv | 1 | |||
| rs72659338 | 1.000 | 0.120 | 7 | 94427654 | missense variant | G/A | snv | 1 | |||
| rs72659345 | 1.000 | 0.120 | 7 | 94430291 | frameshift variant | ATAA/- | delins | 1 |