ClinVar for MedGen (Select 90985) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2506571	NM_003836.7(DLK1):c.67+78C>T	DLK1	Single nucleotide variant (intron variant)	Central precocious puberty	GUncertain significance
Select item 2506570	NM_003836.7(DLK1):c.357C>G (p.Tyr119Ter)	DLK1 (Y119*)	Single nucleotide variant (nonsense)	Central precocious puberty	GLikely pathogenic