"Baylor Genetics"[submitter] AND "HSD17B10"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028768	NM_004493.3(HSD17B10):c.85C>G (p.Arg29Gly)	HSD17B10 (R29G)	Single nucleotide variant (missense variant)	HSD10 mitochondrial disease	GLikely pathogenic
Select item 1028767	NM_004493.3(HSD17B10):c.14G>A (p.Cys5Tyr)	HSD17B10 (C5Y)	Single nucleotide variant (missense variant)	HSD10 mitochondrial disease	GUncertain significance