ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.859-8del

dbSNP: rs2149785367
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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 RCV002146274 SCV002468901 likely benign not provided 2024-08-27 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005248512 SCV005895742 likely benign Hereditary diffuse gastric adenocarcinoma 2024-10-10 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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