ClinVar Miner

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

dbSNP: rs990193541
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae 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

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