ClinVar Miner

Submissions for variant NM_003412.4(ZIC1):c.1311G>T (p.Ala437=)

gnomAD frequency: 0.00001  dbSNP: rs564229372
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000899117 SCV001043366 likely benign not provided 2017-10-09 criteria provided, single submitter clinical testing

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