ClinVar Miner

Submissions for variant NM_015311.3(OBSL1):c.2408-32T>A

dbSNP: rs2303543
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001615775 SCV001836789 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788606 SCV002029263 benign 3M syndrome 2 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615775 SCV005240452 benign not provided criteria provided, single submitter not provided

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