ClinVar Miner

Submissions for variant NM_000424.4(KRT5):c.86G>A (p.Arg29His)

gnomAD frequency: 0.00001  dbSNP: rs543574061
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 RCV002127523 SCV002401930 benign not provided 2023-11-20 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002127523 SCV004235953 uncertain significance not provided 2023-11-16 criteria provided, single submitter clinical testing

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