ClinVar Miner

Submissions for variant NM_004752.4(GCM2):c.679A>G (p.Ile227Val)

gnomAD frequency: 0.00864  dbSNP: rs35395043
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 RCV000975101 SCV001122978 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819148 SCV002069790 benign not specified 2018-11-08 criteria provided, single submitter clinical testing

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