rs74855521
This variant is located in the PCARE gene.
▶ClinVar annotation
About PCARE
The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]
View all PCARE variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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