ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.2355G>A (p.Ser785=)

gnomAD frequency: 0.00285  dbSNP: rs148137322
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194326 SCV000247617 uncertain significance not specified 2015-06-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000914655 SCV001059838 benign not provided 2023-12-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000914655 SCV004146436 likely benign not provided 2022-05-01 criteria provided, single submitter clinical testing INSR: BP4, BP7

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