ClinVar Miner

Submissions for variant NM_007129.5(ZIC2):c.528C>T (p.Asn176=)

gnomAD frequency: 0.00772  dbSNP: rs143055297
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251897 SCV000311718 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000870863 SCV001012420 benign Holoprosencephaly 5 2025-01-27 criteria provided, single submitter clinical testing
GeneDx RCV001711820 SCV001941496 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000870863 SCV002048313 benign Holoprosencephaly 5 2023-10-14 criteria provided, single submitter clinical testing

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