"PreventionGenetics, part of Exact Sciences"[submitter] AND "CLRN2"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2362909	NM_001079827.2(CLRN2):c.206G>A (p.Cys69Tyr)	CLRN2 (C69Y)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3051809	NM_001079827.2(CLRN2):c.235C>T (p.Arg79Cys)	CLRN2 (R79C)	Single nucleotide variant (missense variant)	CLRN2-related disorder	GUncertain significance
Select item 3048511	NM_001079827.2(CLRN2):c.596A>T (p.His199Leu)	CLRN2 (H199L)	Single nucleotide variant (missense variant)	CLRN2-related disorder	GLikely benign

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