ClinVar Miner

Submissions for variant NM_004568.6(SERPINB6):c.750C>T (p.Tyr250=)

gnomAD frequency: 0.00065  dbSNP: rs35617833
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000592905 SCV000701939 uncertain significance not provided 2016-10-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000592905 SCV002382433 benign not provided 2024-09-03 criteria provided, single submitter clinical testing
GeneDx RCV000592905 SCV002498987 likely benign not provided 2021-09-17 criteria provided, single submitter clinical testing

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