"GeneDx"[submitter] AND "MYD88"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1316463	NM_002468.5(MYD88):c.103_104del (p.Leu35fs)	MYD88 (L35fs)	Microsatellite (frameshift variant)	Pyogenic bacterial infections due to MyD88 deficiency +1 more	GConflicting classifications of pathogenicity
Select item 253356	GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	ABHD5, ACAA1 +177 more	Copy number gain	See cases	GLikely pathogenic