ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.653-9_653-7delinsC

dbSNP: rs1568470641
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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) RCV000730034 SCV000857742 benign not specified 2018-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507293 SCV002805185 likely benign Insulin-resistant diabetes mellitus AND acanthosis nigricans; Hyperinsulinism due to INSR deficiency; Leprechaunism syndrome; Rabson-Mendenhall syndrome 2021-09-01 criteria provided, single submitter clinical testing

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