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rs11249215

From SNPedia

Orientationplus
Stabilizedplus
Make rs11249215(A;A)
Make rs11249215(A;G)
Make rs11249215(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position24970693
is asnp
is mentioned by
dbSNPrs11249215
dbSNP (classic)rs11249215
ClinGenrs11249215
ebirs11249215
HLIrs11249215
Exacrs11249215
Gnomadrs11249215
Varsomers11249215
LitVarrs11249215
Maprs11249215
PheGenIrs11249215
Biobankrs11249215
1000 genomesrs11249215
hgdprs11249215
ensemblrs11249215
geneviewrs11249215
scholarrs11249215
googlers11249215
pharmgkbrs11249215
gwascentralrs11249215
openSNPrs11249215
23andMers11249215
SNPshotrs11249215
SNPdbers11249215
MSV3drs11249215
GWAS Ctlgrs11249215
GMAF0.4743
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21743469OA-icon.png]
Trait
Title Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
Risk Allele A
P-val 9E-11
Odds Ratio None None


[PMID 28638311OA-icon.png] A Variant in RUNX3 Is Associated with the Risk of Ankylosing Spondylitis in Koreans.