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rs3826656

From SNPedia

Orientationplus
Stabilizedplus
Make rs3826656(A;A)
Make rs3826656(A;G)
Make rs3826656(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position51223357
GeneCD33
is asnp
is mentioned by
dbSNPrs3826656
ebirs3826656
HLIrs3826656
Exacrs3826656
Varsomers3826656
Maprs3826656
PheGenIrs3826656
hapmaprs3826656
1000 genomesrs3826656
hgdprs3826656
ensemblrs3826656
gopubmedrs3826656
geneviewrs3826656
scholarrs3826656
googlers3826656
pharmgkbrs3826656
gwascentralrs3826656
openSNPrs3826656
23andMers3826656
23andMe allrs3826656
SNP Nexus

SNPshotrs3826656
SNPdbers3826656
MSV3drs3826656
GWAS Ctlgrs3826656
GMAF0.3361
Max Magnitude
? (A;A) (A;G) (G;G) 28
genomeweb rs4420638 rs11159647 and rs3826656 were also significantly associated with Alzheimer's disease
GWAS snp
PMID [PMID 18976728OA-icon.png]
Trait Alzheimer's disease
Title Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE
Risk Allele
P-val 0.000006
Odds Ratio NR NR




[PMID 20574532OA-icon.png] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.


[PMID 22167654] Association studies of 19 candidate SNPs with sporadic Alzheimer's disease in the North Chinese Han population.


GET Evidence
rs3826656
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.71875
summary



[PMID 26455864] Association of CD33 and MS4A cluster variants with Alzheimer's disease in East Asian Populations