ClinVar Miner

Submissions for variant NM_007129.5(ZIC2):c.261C>T (p.Gly87=)

gnomAD frequency: 0.00001  dbSNP: rs1024248405
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002178626 SCV002474653 likely benign Holoprosencephaly 5 2022-06-22 criteria provided, single submitter clinical testing

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