C1orf167
chromosome 1 open reading frame 167
Summary
Implicated in coronary artery disease. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants4 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55738118 | 1:11,838,451 | C/T | intron variant | — |
| rs12134663 | 1:11,838,646 | A/C | intron variant | — |
| rs72640211 | 1:11,838,762 | G/A | coding sequence variant | — |
| rs375481053 | 1:11,849,443 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.