ClinVar Miner

Submissions for variant NM_014345.3(ZNF318):c.6639G>A (p.Ser2213=)

gnomAD frequency: 0.00158  dbSNP: rs139964158
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 RCV000958337 SCV001105172 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000958337 SCV004161680 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing ZNF318: BP4, BP7

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