C15orf39
chromosome 15 open reading frame 39
Summary
Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants20 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143001709 | 15:75,491,778 | G/A | intron variant | — |
| rs746658909 | 15:75,498,429 | A/G | — | uncertain significance |
| rs767798047 | 15:75,498,555 | C/T | — | uncertain significance |
| rs374466401 | 15:75,498,937 | G/T | — | uncertain significance |
| rs151171215 | 15:75,498,943 | C/G | — | likely benign |
| rs749663017 | 15:75,498,970 | T/C | — | uncertain significance |
| rs931279210 | 15:75,499,207 | A/G | — | uncertain significance |
| rs138715960 | 15:75,499,294 | T/A | — | uncertain significance |
| rs748815589 | 15:75,499,315 | G/A | — | uncertain significance |
| rs752910401 | 15:75,499,390 | A/G | — | uncertain significance |
| rs182425183 | 15:75,499,507 | C/T | — | uncertain significance |
| rs370447315 | 15:75,499,642 | A/G | — | uncertain significance |
| rs553765076 | 15:75,499,768 | C/T | — | uncertain significance |
| rs141245544 | 15:75,499,776 | G/A | — | uncertain significance |
| rs150407602 | 15:75,499,927 | G/A | — | uncertain significance |
| rs2542792659 | 15:75,500,052 | C/G | — | uncertain significance |
| rs144091400 | 15:75,500,164 | G/A | — | likely benign |
| rs745391071 | 15:75,500,191 | C/A | — | uncertain significance |
| rs2070454231 | 15:75,500,395 | C/T | — | uncertain significance |
| rs2542794086 | 15:75,500,622 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.