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rs8070463

From SNPedia

Orientationplus
Stabilizedplus
Make rs8070463(C;C)
Make rs8070463(C;T)
Make rs8070463(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position47691470
is asnp
is mentioned by
dbSNPrs8070463
dbSNP (classic)rs8070463
ClinGenrs8070463
ebirs8070463
HLIrs8070463
Exacrs8070463
Gnomadrs8070463
Varsomers8070463
LitVarrs8070463
Maprs8070463
PheGenIrs8070463
Biobankrs8070463
1000 genomesrs8070463
hgdprs8070463
ensemblrs8070463
geneviewrs8070463
scholarrs8070463
googlers8070463
pharmgkbrs8070463
gwascentralrs8070463
openSNPrs8070463
23andMers8070463
SNPshotrs8070463
SNPdbers8070463
MSV3drs8070463
GWAS Ctlgrs8070463
GMAF0.489
Max Magnitude0
? (C;C) (C;T) (T;T) 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 C
P-val 5E-8
Odds Ratio None None
GWAS snp
PMID [PMID 22190364OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Risk Allele T
P-val 1E-7
Odds Ratio 1.1500 None


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


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