ClinVar Miner

Submissions for variant NM_201378.4(PLEC):c.71-11710G>T

dbSNP: rs200335928
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000999104 SCV001155555 uncertain significance not provided 2024-04-01 criteria provided, single submitter clinical testing
Athena Diagnostics RCV004997567 SCV005621798 likely benign not specified 2024-02-14 criteria provided, single submitter clinical testing

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