ClinVar Miner

Submissions for variant NC_000007.14:g.140783126A>G

dbSNP: rs397516887
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
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037907 SCV000061569 likely benign not specified 2010-06-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002513486 SCV003509190 likely benign RASopathy 2023-08-17 criteria provided, single submitter clinical testing

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