"PreventionGenetics, part of Exact Sciences"[submitter] AND "RSPRY1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 720510	NM_133368.3(RSPRY1):c.189C>T (p.Ala63=)	RSPRY1	Single nucleotide variant (synonymous variant)	RSPRY1-related disorder +1 more	GBenign
Select item 789835	NM_133368.3(RSPRY1):c.1191C>T (p.Tyr397=)	RSPRY1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 789836	NM_133368.3(RSPRY1):c.1252A>G (p.Ile418Val)	RSPRY1 (I418V)	Single nucleotide variant (missense variant)	RSPRY1-related disorder +1 more	GBenign

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