ClinVar Miner

List of variants reported as risk factor for Rheumatoid arthritis

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016382.4(CD244):c.834+526A>G rs3766379 0.57260
NM_000246.3(CIITA):c.-286G= rs3087456 0.47237
NM_001144962.2(NFKBIL1):c.-13+590T>A rs2071592 0.37279
NM_003059.3(SLC22A4):c.393+6607C>T rs3792876 0.06888
NM_015967.8(PTPN22):c.1858= (p.Trp620=) rs2476601 0.06839
NM_001014286.3(SUPT20H):c.73A>T (p.Lys25Ter) rs1566328963

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.