ClinVar Miner

Submissions for variant NM_001034852.3(SMOC1):c.858-27del

dbSNP: rs139924326
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
GeneDx RCV001683940 SCV001897852 benign not provided 2021-05-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810230 SCV002057490 benign Microphthalmia with limb anomalies 2021-07-15 criteria provided, single submitter clinical testing

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