rs371765951

This variant is located in the C10orf55 gene.

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ClinVar annotation

Likely Benign
1 submitter

C10orf55-related disorder

View on ClinVar →

About C10orf55

Enables identical protein binding activity. [provided by Alliance of Genome Resources, Jul 2025]

View all C10orf55 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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