ClinVar Miner

Submissions for variant NM_005655.4(KLF10):c.609C>T (p.Ala203=)

gnomAD frequency: 0.00006  dbSNP: rs373356757
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002215716 SCV002373667 likely benign not provided 2023-06-15 criteria provided, single submitter clinical testing

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