ClinVar for MedGen (Select 1823977) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065705	NM_003920.5(TIMELESS):c.909+5G>A	TIMELESS	Single nucleotide variant (intron variant)	Advance sleep phase syndrome, familial, 4	GUncertain significance
Select item 2672272	NM_003920.5(TIMELESS):c.2515G>A (p.Asp839Asn)	TIMELESS (D838N +1 more)	Single nucleotide variant (missense variant +1 more)	Advance sleep phase syndrome, familial, 4	GBenign