ClinVar Miner

Submissions for variant NM_004655.4(AXIN2):c.348A>C (p.Gly116=)

dbSNP: rs896845940
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001444873 SCV001647887 likely benign Oligodontia-cancer predisposition syndrome 2023-05-04 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001444873 SCV005083403 benign Oligodontia-cancer predisposition syndrome 2024-06-26 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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