ClinVar Miner

Submissions for variant NM_002354.3(EPCAM):c.597T>C (p.Ser199=)

dbSNP: rs587780770
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 RCV000123195 SCV000166500 likely benign Lynch syndrome 2014-11-06 no assertion criteria provided clinical testing

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