C0266432[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 827819	NM_000233.4(LHCGR):c.947+4_947+7del	LHCGR, STON1-GTF2A1L	Deletion (intron variant +1 more)	Gonadotropin-independent familial sexual precocity +1 more	GConflicting classifications of pathogenicity
Select item 827820	NM_000233.4(LHCGR):c.233+1G>A	LHCGR, STON1-GTF2A1L	Single nucleotide variant (intron variant +1 more)	Leydig cell agenesis	GLikely pathogenic