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rs116488202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(C;T) 3 likely to carry one HLA-B27 allele, possible risk for B27 Syndromes.
(T;T) 3 likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.
ReferenceGRCh38 38.1/141
Chromosome6
Position31377139
is asnp
is mentioned by
dbSNPrs116488202
ebirs116488202
HLIrs116488202
Exacrs116488202
Varsomers116488202
Maprs116488202
PheGenIrs116488202
hapmaprs116488202
1000 genomesrs116488202
hgdprs116488202
ensemblrs116488202
gopubmedrs116488202
geneviewrs116488202
scholarrs116488202
googlers116488202
pharmgkbrs116488202
gwascentralrs116488202
openSNPrs116488202
23andMers116488202
23andMe allrs116488202
SNP Nexus

SNPshotrs116488202
SNPdbers116488202
MSV3drs116488202
GWAS Ctlgrs116488202
Max Magnitude3

[PMID 25200001] Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis