"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "KLHL41"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 474868	NM_006063.3(KLHL41):c.175C>T (p.Arg59Cys)	KLHL41 (R59C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1163804	NM_006063.3(KLHL41):c.1459A>G (p.Met487Val)	KLHL41 (M487V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 541705	NM_006063.3(KLHL41):c.1562A>G (p.Lys521Arg)	KLHL41 (K521R)	Single nucleotide variant (missense variant)	Nemaline myopathy 9 +1 more	GUncertain significance

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