ClinVar Miner

Submissions for variant NM_001048166.1(STIL):c.2070A>T (p.Ser690=)

dbSNP: rs367887740
Minimum review status: Collection method:
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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) RCV000725981 SCV000340983 uncertain significance not provided 2016-04-12 criteria provided, single submitter clinical testing
GeneDx RCV000725981 SCV000525899 likely benign not provided 2019-09-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000725981 SCV001052703 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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