ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.2091C>G (p.Ile697Met)

dbSNP: rs886051881
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000301104 SCV000396400 uncertain significance Brody myopathy 2016-06-14 criteria provided, single submitter clinical testing

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