"GeneDx"[submitter] AND "RSPRY1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1283466	NM_133368.3(RSPRY1):c.350+60G>A	RSPRY1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1259854	NM_133368.3(RSPRY1):c.351-167dup	RSPRY1	Duplication (intron variant)	not provided	GBenign
Select item 1269982	NM_133368.3(RSPRY1):c.644-224G>C	RSPRY1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253607	NM_133368.3(RSPRY1):c.644-146A>G	RSPRY1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243937	NM_133368.3(RSPRY1):c.703-20dup	RSPRY1	Duplication (intron variant)	not provided	GBenign
Select item 1286559	NM_133368.3(RSPRY1):c.770-169C>G	RSPRY1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289357	NM_133368.3(RSPRY1):c.1161+36T>C	RSPRY1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1262046	NM_133368.3(RSPRY1):c.1162-108A>C	RSPRY1	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar