ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.211C>T (p.His71Tyr)

dbSNP: rs1603270864
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Kariminejad - Najmabadi Pathology & Genetics Center RCV000856703 SCV000999240 uncertain significance Muscle weakness 2018-08-20 criteria provided, single submitter clinical testing

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