ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.1179G>A (p.Gly393=)

gnomAD frequency: 0.00025  dbSNP: rs140573575
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000178735 SCV000230876 uncertain significance not provided 2015-04-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000178735 SCV001080321 likely benign not provided 2024-11-18 criteria provided, single submitter clinical testing

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