ClinVar Miner

Submissions for variant NM_024915.4(GRHL2):c.981G>A (p.Ala327=)

gnomAD frequency: 0.00004  dbSNP: rs368774126
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
Athena Diagnostics RCV000992094 SCV001144090 benign not provided 2019-07-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000992094 SCV005731063 likely benign not provided 2024-04-25 criteria provided, single submitter clinical testing

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