KIAA1958
KIAA1958
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs575537351 | 9:115,249,902 | T/G | — | — |
| rs72762209 | 9:115,254,577 | T/G | intron variant | — |
| rs7865240 | 9:115,255,974 | T/C | regulatory region variant | — |
| rs16917040 | 9:115,282,036 | T/C | intron variant | — |
| rs59289606 | 9:115,325,365 | C/A | intron variant | — |
| rs2540063374 | 9:115,336,523 | G/T | — | uncertain significance |
| rs189232038 | 9:115,336,773 | A/T | — | uncertain significance |
| rs754207055 | 9:115,336,817 | G/C | — | uncertain significance |
| rs540668974 | 9:115,336,844 | C/A | — | uncertain significance |
| rs146645773 | 9:115,336,871 | G/T | — | uncertain significance |
| rs868262809 | 9:115,336,931 | G/A | — | likely benign |
| rs2540064565 | 9:115,337,003 | G/A | — | uncertain significance |
| rs748319120 | 9:115,337,090 | C/T | — | uncertain significance |
| rs1260644697 | 9:115,337,141 | A/T | — | uncertain significance |
| rs372559981 | 9:115,337,166 | T/C | — | uncertain significance |
| rs375756873 | 9:115,337,198 | A/G | — | likely benign |
| rs764169780 | 9:115,337,282 | A/G | — | uncertain significance |
| rs370149959 | 9:115,337,387 | C/G | — | uncertain significance |
| rs2540065786 | 9:115,337,388 | T/G | — | uncertain significance |
| rs528209413 | 9:115,337,516 | G/A | — | uncertain significance |
| rs151038756 | 9:115,373,042 | C/T | intron variant | — |
| rs543043690 | 9:115,385,645 | C/T | — | — |
| rs190086453 | 9:115,385,842 | A/G | intron variant | — |
| rs185445303 | 9:115,408,796 | A/G | intron variant | — |
| rs10981466 | 9:115,409,875 | A/T | intron variant | — |
| rs189253264 | 9:115,417,203 | C/T | intron variant | — |
| rs754061043 | 9:115,421,850 | G/A | — | uncertain significance |
| rs775979828 | 9:115,422,279 | G/A | — | uncertain significance |
| rs767763928 | 9:115,422,322 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.