ClinVar Miner

Submissions for variant NM_003502.4(AXIN1):c.2186+7C>T

gnomAD frequency: 0.00833  dbSNP: rs189357878
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514030 SCV000611001 likely benign not provided 2017-09-27 criteria provided, single submitter clinical testing
Invitae RCV000514030 SCV001101404 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000514030 SCV004131664 benign not provided 2022-04-01 criteria provided, single submitter clinical testing AXIN1: BP4, BS1, BS2

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