Related gene-specific medical variations for Gene (Select 10324) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689321	NM_006063.3(KLHL41):c.1666G>A (p.Glu556Lys)	KLHL41 (E556K)	Single nucleotide variant (missense variant)	Nemaline myopathy 9	GUncertain significance
Select item 2689320	NM_006063.3(KLHL41):c.427C>T (p.Leu143Phe)	KLHL41 (L143F)	Single nucleotide variant (missense variant)	Nemaline myopathy 9	GUncertain significance
Select item 2433166	NM_006063.3(KLHL41):c.1432C>G (p.Leu478Val)	KLHL41 (L478V)	Single nucleotide variant (missense variant)	Nemaline myopathy 9	GUncertain significance

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