FGF19[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2513754	NM_005117.3(FGF19):c.253G>A (p.Val85Ile)	FGF19 (V85I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410681	NM_005117.3(FGF19):c.119A>G (p.Asp40Gly)	FGF19 (D40G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094704	NM_005117.3(FGF19):c.89C>G (p.Ala30Gly)	FGF19 (A30G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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