ClinVar for MedGen (Select 886756) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1687715	NM_003076.5(SMARCD1):c.1051C>T (p.Arg351Cys)	SMARCD1 (R351C)	Single nucleotide variant (missense variant)	Alopecia, androgenetic, 1	GLikely pathogenic
Select item 1687627	NM_001453.3(FOXC1):c.1450C>T (p.His484Tyr)	FOXC1 (H484Y)	Single nucleotide variant (missense variant)	Alopecia, androgenetic, 1	GUncertain significance