ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.*4A>T

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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. RCV004788740 SCV005402887 benign Hereditary diffuse gastric adenocarcinoma 2024-09-25 criteria provided, single submitter clinical testing This variant is considered benign. This variant occurs in the non-coding 3' untranslated region of the gene, and is not expected to impact protein function.

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