ClinVar Miner

Submissions for variant NM_003922.4(HERC1):c.2768A>G (p.Asn923Ser)

gnomAD frequency: 0.01265  dbSNP: rs35978932
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 RCV001574177 SCV001800942 likely benign not provided 2021-04-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001574177 SCV002331048 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001574177 SCV005215078 likely benign not provided criteria provided, single submitter not provided

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