ClinVar Miner

Submissions for variant NM_000875.5(IGF1R):c.-41_-33del

dbSNP: rs544674838
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000342071 SCV000483528 benign Growth delay due to insulin-like growth factor I resistance 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000342071 SCV002801679 likely benign Growth delay due to insulin-like growth factor I resistance 2021-11-16 criteria provided, single submitter clinical testing

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