ClinVar Miner

List of variants in gene SHOX reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000451.4(SHOX):c.277+17T>G rs2239402 0.97040
NM_000451.4(SHOX):c.63C>T (p.Gly21=) rs142306835 0.00472
NM_006883.2(SHOX):c.-432-96G>A rs188327789

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.