ClinVar Miner

Submissions for variant NM_016366.3(CABP2):c.201C>A (p.Ala67=)

dbSNP: rs138981491
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000592996 SCV000708528 uncertain significance not provided 2017-05-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000592996 SCV001039196 likely benign not provided 2024-11-29 criteria provided, single submitter clinical testing
GeneDx RCV000592996 SCV001796293 likely benign not provided 2021-05-05 criteria provided, single submitter clinical testing

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