ClinVar Miner

Submissions for variant NM_032805.3(ZSCAN10):c.768G>A (p.Ala256=)

gnomAD frequency: 0.00277  dbSNP: rs72772561
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000950247 SCV001096537 benign not provided 2017-05-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000950247 SCV004144867 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing ZSCAN10: BP4, BP7, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000950247 SCV005293840 benign not provided criteria provided, single submitter not provided

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