ClinVar Miner

List of variants reported as risk factor for arthritis by OMIM

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
HLA-B, HLA-B27
NFKBIL1, -62T-A
NM_000246.3(CIITA):c.-286G= rs3087456
NM_000557.5(GDF5):c.-275= rs143383
NM_001159740.2(LTA):c.-9-198A>G rs909253
NM_001463.4(FRZB):c.598C>T (p.Arg200Trp) rs288326
NM_001463.4(FRZB):c.970C>G (p.Arg324Gly) rs7775
NM_015967.7(PTPN22):c.1858C>T (p.Arg620Trp) rs2476601
NM_016382.4(CD244):c.834+526A>G rs3766379
SLC22A4, IVS1, T-C
TNF, -308G-A

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.