ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.1861+27C>T

gnomAD frequency: 0.21056  dbSNP: rs3815902
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001662510 SCV000604034 benign not provided 2019-09-11 criteria provided, single submitter clinical testing
GeneDx RCV001662510 SCV001874658 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730699 SCV001981323 benign Leprechaunism syndrome 2021-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730700 SCV001981334 benign Rabson-Mendenhall syndrome 2021-08-19 criteria provided, single submitter clinical testing

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