"Ambry Genetics"[submitter] AND "LOC126807431"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3083087	NM_013391.3(DMGDH):c.2566C>T (p.Arg856Trp)	DMGDH, LOC126807431 (R856W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083086	NM_013391.3(DMGDH):c.2450A>T (p.Tyr817Phe)	DMGDH, LOC126807431 (Y817F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance