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rs868213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs868213(C;C)
Make rs868213(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67186554
GeneEXOC3L1
is asnp
is mentioned by
dbSNPrs868213
ebirs868213
HLIrs868213
Exacrs868213
Varsomers868213
Maprs868213
PheGenIrs868213
hapmaprs868213
1000 genomesrs868213
hgdprs868213
ensemblrs868213
gopubmedrs868213
geneviewrs868213
scholarrs868213
googlers868213
pharmgkbrs868213
gwascentralrs868213
openSNPrs868213
23andMers868213
23andMe allrs868213
SNP Nexus

SNPshotrs868213
SNPdbers868213
MSV3drs868213
GWAS Ctlgrs868213
GMAF0.1492
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19854717OA-icon.png] The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)

23andMe reports that each G allele at rs868213 appears to be associated with 1.5x higher odds of ankylosing spondylitis. [PMID 19854717OA-icon.png]