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rs34826052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34826052(G;T)
Make rs34826052(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position35345697
GeneCD22
is asnp
is mentioned by
dbSNPrs34826052
ebirs34826052
HLIrs34826052
Exacrs34826052
Varsomers34826052
Maprs34826052
PheGenIrs34826052
hapmaprs34826052
1000 genomesrs34826052
hgdprs34826052
ensemblrs34826052
gopubmedrs34826052
geneviewrs34826052
scholarrs34826052
googlers34826052
pharmgkbrs34826052
gwascentralrs34826052
openSNPrs34826052
23andMers34826052
23andMe allrs34826052
SNP Nexus

SNPshotrs34826052
SNPdbers34826052
MSV3drs34826052
GWAS Ctlgrs34826052
GMAF0.05601
Max Magnitude0

[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis


[PMID 21247474OA-icon.png] Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.