ClinVar Miner

Submissions for variant NM_002354.3(EPCAM):c.859-6A>C

dbSNP: rs150307203
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000123200 SCV000166505 likely benign Lynch syndrome 2014-11-06 no assertion criteria provided clinical testing

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