ClinVar Miner

List of variants studied for bone remodeling disease by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003052.5(SLC34A1):c.56G>A (p.Arg19His) rs765766600 0.00006
NM_020832.3(ZNF687):c.1695C>G (p.His565Gln) rs777840812 0.00004
NM_002546.4(TNFRSF11B):c.884T>C (p.Leu295Pro) rs1586952570
NM_020832.3(ZNF687):c.2810C>A (p.Pro937His) rs148402804

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.