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rs424232

From SNPedia

Orientationminus
Stabilizedminus
Make rs424232(A;A)
Make rs424232(A;G)
Make rs424232(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32240547
is asnp
is mentioned by
dbSNPrs424232
ebirs424232
HLIrs424232
Exacrs424232
Varsomers424232
Maprs424232
PheGenIrs424232
hapmaprs424232
1000 genomesrs424232
hgdprs424232
ensemblrs424232
gopubmedrs424232
geneviewrs424232
scholarrs424232
googlers424232
pharmgkbrs424232
gwascentralrs424232
openSNPrs424232
23andMers424232
23andMe allrs424232
SNP Nexus

SNPshotrs424232
SNPdbers424232
MSV3drs424232
GWAS Ctlgrs424232
GMAF0.2961
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 23053058] Search for schizophrenia susceptibility variants at the HLA-DRB1 locus among a British population

GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele C
P-val 5E-21
Odds Ratio NR NR