Related gene-specific medical variations for Gene (Select 10184) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290599	NM_005779.3(LHFPL2):c.175C>T (p.Pro59Ser)	LHFPL2, LOC129994111 (P59S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118618	NM_005779.3(LHFPL2):c.157T>G (p.Ser53Ala)	LHFPL2, LOC129994111 (S53A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532615	NM_005779.3(LHFPL2):c.205C>T (p.Arg69Trp)	LHFPL2, LOC129994111 (R69W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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