List of variants in gene LDHD reported as likely pathogenic for Lactic aciduria due to D-lactic acid

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_194436.3(LDHD):c.1319C>T (p.Thr440Met)	rs764877688	0.00012
NM_194436.3(LDHD):c.1053G>T (p.Trp351Cys)	rs1567502487
NM_194436.3(LDHD):c.561_562del (p.Leu188fs)

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