"Fulgent Genetics, Fulgent Genetics"[submitter] AND "AMPD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 92338	NM_000036.3(AMPD1):c.860A>T (p.Lys287Ile)	AMPD1 (K320I +2 more)	Single nucleotide variant (missense variant)	Muscle AMP deaminase deficiency +4 more	GConflicting classifications of pathogenicity
Select item 197620	NM_000036.3(AMPD1):c.468G>T (p.Gln156His)	AMPD1 (Q189H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity