ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.29C>G (p.Ser10Cys)

dbSNP: rs1603270381
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine RCV001007860 SCV001167558 uncertain significance X-linked scapuloperoneal muscular dystrophy no assertion criteria provided research

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