ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1008+8G>T

dbSNP: rs990193541
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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 RCV000989621 SCV001065909 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-27 criteria provided, single submitter clinical testing
Mendelics RCV000989621 SCV001140138 uncertain significance Hereditary diffuse gastric adenocarcinoma 2019-05-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000989621 SCV005407079 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-17 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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