rs372770167
This is a synonymous variant in the ARMC9 gene — it does not change the protein's amino acid sequence.
▶ClinVar annotation
Likely Benign★☆☆☆
4 submitters2 publicationsARMC9-related Joubert syndrome; Joubert syndrome 30; Joubert syndrome; not provided
View on ClinVar →About ARMC9
Predicted to be involved in cilium assembly and positive regulation of smoothened signaling pathway. Located in centriole and ciliary basal body. Implicated in Joubert syndrome 30. [provided by Alliance of Genome Resources, Jul 2025]
View all ARMC9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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