ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1321-10T>C

dbSNP: rs1597897718
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001455183 SCV001658938 likely benign Hereditary diffuse gastric adenocarcinoma 2021-08-30 criteria provided, single submitter clinical testing
GeneDx RCV000928196 SCV001826421 likely benign not provided 2020-09-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001455183 SCV005405154 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-18 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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