COMMD10
COMM domain containing 10
Summary
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants16 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759898407 | 5:115,420,759 | C/T | — | likely benign |
| rs944366806 | 5:115,423,196 | T/C | — | uncertain significance |
| rs149347900 | 5:115,423,228 | G/C | — | uncertain significance |
| rs768965375 | 5:115,423,258 | C/T | — | uncertain significance |
| rs17138866 | 5:115,424,611 | T/C | upstream gene variant | — |
| rs146111323 | 5:115,426,819 | C/T | — | likely benign |
| rs765803405 | 5:115,428,371 | C/T | — | uncertain significance |
| rs373245497 | 5:115,469,863 | T/A | — | uncertain significance |
| rs1396485 | 5:115,512,352 | G/A | intron variant | — |
| rs7709377 | 5:115,540,573 | A/T | — | — |
| rs253959 | 5:115,568,757 | T/G | — | — |
| rs4466200 | 5:115,596,152 | G/A | intron variant | — |
| rs10043228 | 5:115,597,048 | C/G | — | — |
| rs2532006079 | 5:115,627,259 | G/T | — | uncertain significance |
| rs749541250 | 5:115,627,265 | T/C | — | uncertain significance |
| rs148262275 | 5:115,628,152 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.