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rs13202464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 3 likely to be a carrier of one HLA-B27 allele, possible risk for B27 Syndromes.
(G;G) 3 likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes.
ReferenceGRCh38 38.1/141
Chromosome6
Position31376806
GeneFGFR3P1
is asnp
is mentioned by
dbSNPrs13202464
dbSNP (classic)rs13202464
ClinGenrs13202464
ebirs13202464
HLIrs13202464
Exacrs13202464
Gnomadrs13202464
Varsomers13202464
LitVarrs13202464
Maprs13202464
PheGenIrs13202464
Biobankrs13202464
1000 genomesrs13202464
hgdprs13202464
ensemblrs13202464
geneviewrs13202464
scholarrs13202464
googlers13202464
pharmgkbrs13202464
gwascentralrs13202464
openSNPrs13202464
23andMers13202464
SNPshotrs13202464
SNPdbers13202464
MSV3drs13202464
GWAS Ctlgrs13202464
GMAF0.06152
Max Magnitude3
? (A;A) (A;G) (G;G) 28


See: HLA-B27 Syndromes.

Not all alleles of HLA-B27 are at risk for B27 Syndromes, please check the HLA-B27 page for details.

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[PMID 31523044] Analysis of 47 non-MHC Ankylosing Spondylitis Susceptibility Loci Reveals Shared Associated Variants across Caucasians and Han Chinese.