ClinVar Miner

Submissions for variant NM_000208.4(INSR):c.*926_*927insG

gnomAD frequency: 0.00001  dbSNP: rs886054676
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000403463 SCV000415354 uncertain significance Rabson-Mendenhall syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000315470 SCV000415355 uncertain significance Leprechaunism syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000367721 SCV000415356 uncertain significance Insulin-resistant diabetes mellitus AND acanthosis nigricans 2016-06-14 criteria provided, single submitter clinical testing

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