Related gene-specific medical variations for Gene (Select 10554) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3096355	NM_006411.4(AGPAT1):c.809G>A (p.Arg270Gln)	AGPAT1, LOC126859655 (R274Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546642	NM_006411.4(AGPAT1):c.788G>A (p.Arg263Gln)	AGPAT1, LOC126859655	Single nucleotide variant (missense variant)	not specified	GUncertain significance