rs10483724
This is a intron variant variant in the C14orf39 gene.
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]
View all C14orf39 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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