ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.700-20A>T

dbSNP: rs112871502
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 RCV002124881 SCV002410878 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002124881 SCV005285536 benign not provided criteria provided, single submitter not provided

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