ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.2267+17C>T

gnomAD frequency: 0.04450  dbSNP: rs41509747
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811569 SCV001157390 benign not provided 2021-02-04 criteria provided, single submitter clinical testing
Invitae RCV001811569 SCV002407355 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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