"Fulgent Genetics, Fulgent Genetics"[submitter] AND "AGBL5"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 771695	NM_021831.6(AGBL5):c.2046T>A (p.Ser682=)	AGBL5	Single nucleotide variant (synonymous variant +1 more)	Retinitis pigmentosa 75 +1 more	GBenign
Select item 789558	NM_021831.6(AGBL5):c.2375G>A (p.Arg792Gln)	AGBL5 (R792Q)	Single nucleotide variant (missense variant +1 more)	Retinitis pigmentosa 75 +1 more	GBenign/Likely benign