rs139054454

This variant is located in the C14orf39 gene.

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ClinVar annotation

Likely Benign★☆☆☆

1 submitter

About C14orf39

Involved in homologous chromosome pairing at meiosis. Predicted to be located in chromosome. Predicted to be active in central element. Implicated in primary ovarian insufficiency 18 and spermatogenic failure 52. [provided by Alliance of Genome Resources, Jul 2025]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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