ClinVar Miner

Submissions for variant NM_004655.4(AXIN2):c.1060-10C>T

gnomAD frequency: 0.00004  dbSNP: rs376505336
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720030 SCV000517234 likely benign not provided 2020-12-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000472048 SCV000559521 likely benign Oligodontia-cancer predisposition syndrome 2025-01-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258887 SCV002537565 likely benign Hereditary cancer-predisposing syndrome 2021-02-17 criteria provided, single submitter curation
Myriad Genetics, Inc. RCV000472048 SCV005403191 likely benign Oligodontia-cancer predisposition syndrome 2024-07-01 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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