rs116488202
From SNPedia
Orientation | plus |
Stabilized | plus |
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. |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31377139 |
is a | snp |
is | mentioned by |
dbSNP | rs116488202 |
dbSNP (classic) | rs116488202 |
ClinGen | rs116488202 |
ebi | rs116488202 |
HLI | rs116488202 |
Exac | rs116488202 |
Gnomad | rs116488202 |
Varsome | rs116488202 |
LitVar | rs116488202 |
Map | rs116488202 |
PheGenI | rs116488202 |
Biobank | rs116488202 |
1000 genomes | rs116488202 |
hgdp | rs116488202 |
ensembl | rs116488202 |
geneview | rs116488202 |
scholar | rs116488202 |
rs116488202 | |
pharmgkb | rs116488202 |
gwascentral | rs116488202 |
openSNP | rs116488202 |
23andMe | rs116488202 |
SNPshot | rs116488202 |
SNPdbe | rs116488202 |
MSV3d | rs116488202 |
GWAS Ctlg | rs116488202 |
Max Magnitude | 3 |
[PMID 25200001] Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis