Related gene-specific medical variations for Gene (Select 4615) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3246904	NC_000003.11:g.(?_38180153)_(38182777_?)del	MYD88	Deletion	Pyogenic bacterial infections due to MyD88 deficiency	GPathogenic
Select item 2576053	NM_002468.5(MYD88):c.244C>T (p.Pro82Ser)	MYD88 (P82S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 134870	NM_002468.5(MYD88):c.38C>A (p.Pro13Gln)	MYD88 (P13Q)	Single nucleotide variant (missense variant)	not specified	Gnot provided

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