ClinVar Miner

Submissions for variant NM_172056.2(KCNH2):c.1332G>T (p.Glu444Asp) (rs9770044)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Cardiovascular Biomedical Research Unit,Royal Brompton & Harefield NHS Foundation Trust	RCV000057895	SCV000089415	not provided	not provided		no assertion provided	literature only	This variant has been reported in the following publications (PMID:12442276).

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