C1865926[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65758	NM_145239.3(PRRT2):c.649dup (p.Arg217fs)	MVP-DT, PRRT2 (R217fs)	Duplication (frameshift variant)	Seizure +13 more	GPathogenic/Likely pathogenic
Select item 932548	NM_145239.3(PRRT2):c.880-34G>A	MVP-DT, PRRT2	Single nucleotide variant (3 prime UTR variant +1 more)	Episodic kinesigenic dyskinesia +4 more	GPathogenic/Likely pathogenic