ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.4098C>T (p.Ile1366=)

gnomAD frequency: 0.00001  dbSNP: rs1027609786
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817156 SCV002068791 uncertain significance not specified 2017-08-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003718432 SCV004514769 likely benign not provided 2024-02-23 criteria provided, single submitter clinical testing

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