ClinVar Miner

Submissions for variant NM_001174096.2(ZEB1):c.2717C>G (p.Ala906Gly)

gnomAD frequency: 0.00162  dbSNP: rs78449005
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002120746 SCV002433331 benign not provided 2023-10-29 criteria provided, single submitter clinical testing
Mendelics RCV002246684 SCV002516185 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing

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