List of variants in gene GHR, LOC107963950 studied for Laron syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000163.5(GHR):c.-164A>G	rs2940928	0.81907
NM_000163.5(GHR):c.-39G>C	rs527709793	0.00851
NM_000163.5(GHR):c.-176A>G	rs1314535276	0.00004
NM_000163.5(GHR):c.-118C>T	rs1050201240
NM_000163.5(GHR):c.-150C>A	rs368929640
NM_000163.5(GHR):c.-74C>T	rs892049573
NM_000163.5(GHR):c.-76C>T	rs1742723526
NM_000163.5(GHR):c.-89G>T	rs1033209852

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.