Related gene-specific medical variations for Gene (Select 80339) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3216047	NM_025225.3(PNPLA3):c.1250C>T (p.Ser417Phe)	LOC121627950, PNPLA3 (S417F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 902436	NM_025225.3(PNPLA3):c.1262C>T (p.Pro421Leu)	LOC121627950, PNPLA3 (P421L)	Single nucleotide variant (missense variant)	NAFLD1 +1 more	GUncertain significance