ClinVar Miner

Submissions for variant NM_004655.4(AXIN2):c.1907+17G>A

gnomAD frequency: 0.00010  dbSNP: rs201487132
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001638473 SCV001850109 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072945 SCV002373597 likely benign Oligodontia-cancer predisposition syndrome 2024-01-24 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268542 SCV002551250 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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