ClinVar Miner

Submissions for variant NM_172056.2(KCNH2):c.559G>A (p.Gly187Ser) (rs199472867)

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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 RCV000058240 SCV000089760 not provided not provided no assertion provided literature only This variant has been reported in the following publications (PMID:14661677;PMID:19841300).

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