ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2439+1G>T

dbSNP: rs1567516230
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709399 SCV000839097 likely pathogenic Hereditary diffuse gastric adenocarcinoma 2018-07-02 criteria provided, single submitter clinical testing
Laboratory for Genotyping Development, RIKEN RCV003165937 SCV002758160 pathogenic Gastric cancer 2021-07-01 no assertion criteria provided research

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