ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.1050G>A (p.Ser350=)

gnomAD frequency: 0.00003  dbSNP: rs751541632
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
Invitae RCV000912719 SCV001057834 likely benign not provided 2018-03-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000912719 SCV004146438 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing INSR: BP4, BP7

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