ClinVar Miner

Submissions for variant NM_000515.5(GH1):c.387C>T (p.Tyr129=)

gnomAD frequency: 0.00009  dbSNP: rs370785603
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000178108 SCV000230109 uncertain significance not provided 2015-02-17 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001128610 SCV001288077 uncertain significance Decreased response to growth hormone stimulation test 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Labcorp Genetics (formerly Invitae), Labcorp RCV000178108 SCV003208571 likely benign not provided 2024-05-24 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005237660 SCV005886042 likely benign not specified 2025-02-18 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.