ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.5225-22AT[8]

dbSNP: rs113854298
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000969951 SCV001117502 benign not provided 2019-03-05 criteria provided, single submitter clinical testing
GeneDx RCV000969951 SCV001790541 likely benign not provided 2019-10-06 criteria provided, single submitter clinical testing

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