ClinVar Miner

Submissions for variant NM_015311.3(OBSL1):c.1283-9G>A

gnomAD frequency: 0.00022  dbSNP: rs376967214
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000388984 SCV000341463 uncertain significance not provided 2016-06-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000388984 SCV001660285 likely benign not provided 2023-11-18 criteria provided, single submitter clinical testing

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