ClinVar Miner

Submissions for variant NM_001318895.3(FHL2):c.823T>G (p.Cys275Gly)

dbSNP: rs730880110
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000157238 SCV000206965 uncertain significance Primary dilated cardiomyopathy 2014-09-29 no assertion criteria provided clinical testing

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