ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.589-72A>G

gnomAD frequency: 0.00062  dbSNP: rs28363405
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004705041 SCV005225867 likely benign not provided criteria provided, single submitter not provided
University of Washington Department of Laboratory Medicine, University of Washington RCV000209371 SCV000265167 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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