ClinVar Miner

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

dbSNP: rs367887740
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000981840 SCV001129848 likely benign not provided 2018-12-18 criteria provided, single submitter clinical testing

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