C3552574[trait identifier] AND "ARUP Laboratories, Molecular Genetics - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 218825	NM_033163.5(FGF8):c.445-62G>A	FGF8	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1271093	NM_033163.5(FGF8):c.444+19G>A	FGF8	Single nucleotide variant (intron variant)	Hypogonadotropic hypogonadism 6 with or without anosmia +1 more	GBenign
Select item 545463	NM_033163.5(FGF8):c.86_103dup (p.Gly29_Arg34dup)	FGF8	Duplication (inframe_insertion +1 more)	Holoprosencephaly sequence +3 more	GConflicting classifications of pathogenicity

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