ClinVar Miner

Submissions for variant NM_001386125.1(OBSCN):c.20934C>T (p.Ala6978=)

gnomAD frequency: 0.01505  dbSNP: rs1188715
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 RCV000967939 SCV001115364 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000967939 SCV005284123 benign not provided criteria provided, single submitter not provided

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