ClinVar Miner

Submissions for variant NM_000079.4(CHRNA1):c.710A>T (p.Asn237Ile)

dbSNP: rs1558911753
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000678787 SCV000804967 uncertain significance Epilepsy 2017-09-05 no assertion criteria provided clinical testing

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