ClinVar (all) for Orgtrack (Select 506749) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 586969	NM_194436.3(LDHD):c.1319C>T (p.Thr440Met)	LDHD (T463M +1 more)	Single nucleotide variant (missense variant)	Lactic aciduria due to D-lactic acid	GLikely pathogenic
Select item 586968	NM_194436.3(LDHD):c.1053G>T (p.Trp351Cys)	LDHD (W374C +1 more)	Single nucleotide variant (missense variant)	Lactic aciduria due to D-lactic acid	GLikely pathogenic