ClinVar Miner

Submissions for variant NM_000515.5(GH1):c.-63A>T

dbSNP: rs695
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000302385 SCV000483653 likely benign Isolated congenital growth hormone deficiency 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001707687 SCV001934946 benign not provided 2021-06-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707687 SCV005211213 likely benign not provided criteria provided, single submitter not provided

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