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rs10406069

From SNPedia

Orientationplus
Stabilizedplus
Make rs10406069(A;A)
Make rs10406069(A;G)
Make rs10406069(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35345627
GeneCD22
is asnp
is mentioned by
dbSNPrs10406069
ebirs10406069
HLIrs10406069
Exacrs10406069
Varsomers10406069
Maprs10406069
PheGenIrs10406069
hapmaprs10406069
1000 genomesrs10406069
hgdprs10406069
ensemblrs10406069
gopubmedrs10406069
geneviewrs10406069
scholarrs10406069
googlers10406069
pharmgkbrs10406069
gwascentralrs10406069
openSNPrs10406069
23andMers10406069
23andMe allrs10406069
SNP Nexus

SNPshotrs10406069
SNPdbers10406069
MSV3drs10406069
GWAS Ctlgrs10406069
GMAF0.1442
Max Magnitude
? (A;A) (A;G) (G;G) 28

[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.


GET Evidence
CD22-G657D
aa_change Gly657Asp
aa_change_short G657D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary