ClinVar Miner

Submissions for variant NM_000459.5(TEK):c.365-19G>A

gnomAD frequency: 0.00023  dbSNP: rs371486685
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811816 SCV002047829 likely benign not provided 2021-08-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001811816 SCV004686852 benign not provided 2023-06-21 criteria provided, single submitter clinical testing

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