Related gene-specific medical variations for Gene (Select 5360) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 338543	NM_000308.4(CTSA):c.*320G>A	CTSA, PLTP	Single nucleotide variant (3 prime UTR variant +1 more)	Combined deficiency of sialidase AND beta galactosidase	GUncertain significance
Select item 338542	NM_000308.4(CTSA):c.*266T>A	PLTP, CTSA	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 13634	NC_000020.11:g.45919554C>T	PLTP	Single nucleotide variant	RECLASSIFIED - PLTP POLYMORPHISM	GBenign

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