ClinVar Miner

Submissions for variant NM_005378.6(MYCN):c.1171C>A (p.Arg391Ser)

dbSNP: rs1662856733
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV001252328 SCV001428080 likely pathogenic Feingold syndrome type 1 2019-01-01 no assertion criteria provided clinical testing

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