ClinVar Miner

Submissions for variant NM_005445.4(SMC3):c.350+21dup

dbSNP: rs200378516
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002967813 SCV003289745 benign Cornelia de Lange syndrome 3 2025-12-08 criteria provided, single submitter clinical testing

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