ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.2193-9TCT[3]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV005247588 SCV005899690 likely benign Hereditary diffuse gastric adenocarcinoma 2024-10-15 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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