ClinVar Miner

Submissions for variant NM_021224.6(ZNF462):c.3666T>C (p.Asn1222=)

gnomAD frequency: 0.45895  dbSNP: rs3814540
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001732539 SCV001982741 benign not provided 2021-10-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243453 SCV002514237 benign Weiss-Kruszka syndrome 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001732539 SCV005268107 benign not provided criteria provided, single submitter not provided

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