ClinVar Miner

Submissions for variant NM_000406.3(GNRHR):c.523-15del

dbSNP: rs569763619
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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 RCV000270618 SCV000450926 uncertain significance Isolated GnRH Deficiency 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002520263 SCV003032177 benign not provided 2023-06-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002520263 SCV005190128 uncertain significance not provided criteria provided, single submitter not provided

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