ClinVar for MedGen (Select 815313) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 50860	NM_003867.4(FGF17):c.560A>G (p.Asn187Ser)	FGF17 (N187S +1 more)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism 20 with or without anosmia	GPathogenic
Select item 50858	NM_003867.4(FGF17):c.323T>C (p.Ile108Thr)	FGF17 (I108T +1 more)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism 20 with or without anosmia	Grisk factor