rs375481053

This variant is located in the C1orf167 gene.

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ClinVar annotation

Likely Benign★☆☆☆
1 submitter
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About C1orf167

Implicated in coronary artery disease. [provided by Alliance of Genome Resources, Jul 2025]

View all C1orf167 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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