Related gene-specific medical variations for Gene (Select 283748) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2318403	NM_178034.4(PLA2G4D):c.445A>G (p.Asn149Asp)	LOC125078065, PLA2G4D (N149D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2289696	NM_178034.4(PLA2G4D):c.459C>A (p.Asn153Lys)	LOC125078065, PLA2G4D (N153K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance