Have questions? Visit https://www.reddit.com/r/SNPedia

rs11159647

From SNPedia

Orientationplus
Stabilizedplus
Make rs11159647(A;A)
Make rs11159647(A;G)
Make rs11159647(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position84308865
is asnp
is mentioned by
dbSNPrs11159647
ebirs11159647
HLIrs11159647
Exacrs11159647
Varsomers11159647
Maprs11159647
PheGenIrs11159647
hapmaprs11159647
1000 genomesrs11159647
hgdprs11159647
ensemblrs11159647
gopubmedrs11159647
geneviewrs11159647
scholarrs11159647
googlers11159647
pharmgkbrs11159647
gwascentralrs11159647
openSNPrs11159647
23andMers11159647
23andMe allrs11159647
SNP Nexus

SNPshotrs11159647
SNPdbers11159647
MSV3drs11159647
GWAS Ctlgrs11159647
GMAF0.2759
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 0.000002
Odds Ratio NR NR




[PMID 19640594OA-icon.png] Recent insights into the molecular genetics of dementia.


[PMID 20061627OA-icon.png] Genome-wide scan of copy number variation in late-onset Alzheimer's disease.


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


GET Evidence
rs11159647
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary