ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.2575C>T (p.His859Tyr) (rs149536206)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000897981 SCV001042162 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Personalized Diabetes Medicine Program,University of Maryland School of Medicine RCV001174370 SCV001337508 likely benign Monogenic diabetes 2018-01-05 criteria provided, single submitter research ACMG criteria: PP3 (2 predictors), BP4 (6 predictors), BS2 (10 cases and 15 controls in type2diabetesgenetics.org and 1 homozygote in gnomAD)=likely benign

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