"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255607	NM_000233.4(LHCGR):c.1065T>C (p.Asp355=)	STON1-GTF2A1L, LHCGR	Single nucleotide variant (synonymous variant +1 more)	not specified +4 more	GBenign
Select item 255609	NM_000233.4(LHCGR):c.935A>G (p.Asn312Ser)	LHCGR, STON1-GTF2A1L (N312S)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign
Select item 255608	NM_000233.4(LHCGR):c.866+8G>A	STON1-GTF2A1L, LHCGR	Single nucleotide variant (intron variant)	not provided +4 more	GBenign

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