ClinVar Miner

Submissions for variant NM_014915.3(ANKRD26):c.513T>C (p.Asn171=)

gnomAD frequency: 0.00001  dbSNP: rs745670666
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817549 SCV002068816 uncertain significance not specified 2018-03-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542540 SCV003466269 likely benign not provided 2024-07-25 criteria provided, single submitter clinical testing

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