Related gene-specific medical variations for Gene (Select 9965) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3094703	NM_005117.3(FGF19):c.580A>G (p.Thr194Ala)	FGF19, LOC124500681 (T194A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605827	NM_005117.3(FGF19):c.613G>C (p.Gly205Arg)	FGF19, LOC124500681 (G205R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592534	NM_005117.3(FGF19):c.367G>A (p.Glu123Lys)	FGF19, LOC124500681 (E123K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401907	NM_005117.3(FGF19):c.419G>A (p.Arg140His)	FGF19, LOC124500681 (R140H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2358189	NM_005117.3(FGF19):c.613G>A (p.Gly205Arg)	FGF19, LOC124500681 (G205R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341241	NM_005117.3(FGF19):c.550G>A (p.Glu184Lys)	FGF19, LOC124500681 (E184K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328845	NM_005117.3(FGF19):c.347C>G (p.Ser116Trp)	FGF19, LOC124500681 (S116W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247910	NM_005117.3(FGF19):c.535C>T (p.Leu179Phe)	FGF19, LOC124500681 (L179F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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