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rs1326986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1326986(A;G)
Make rs1326986(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position19640584
GeneMALRD1
is asnp
is mentioned by
dbSNPrs1326986
ebirs1326986
HLIrs1326986
Exacrs1326986
Varsomers1326986
Maprs1326986
PheGenIrs1326986
hapmaprs1326986
1000 genomesrs1326986
hgdprs1326986
ensemblrs1326986
gopubmedrs1326986
geneviewrs1326986
scholarrs1326986
googlers1326986
pharmgkbrs1326986
gwascentralrs1326986
openSNPrs1326986
23andMers1326986
23andMe allrs1326986
SNP Nexus

SNPshotrs1326986
SNPdbers1326986
MSV3drs1326986
GWAS Ctlgrs1326986
GMAF0.02479
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062062OA-icon.png]
Trait Ankylosing spondylitis
Title Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
Risk Allele C
P-val 0.000004
Odds Ratio 1.90 [1.58-2.29]