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rs6922617

From SNPedia

Orientationplus
Stabilizedplus
Make rs6922617(A;A)
Make rs6922617(A;G)
Make rs6922617(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position41368363
is asnp
is mentioned by
dbSNPrs6922617
ebirs6922617
HLIrs6922617
Exacrs6922617
Varsomers6922617
Maprs6922617
PheGenIrs6922617
hapmaprs6922617
1000 genomesrs6922617
hgdprs6922617
ensemblrs6922617
gopubmedrs6922617
geneviewrs6922617
scholarrs6922617
googlers6922617
pharmgkbrs6922617
gwascentralrs6922617
openSNPrs6922617
23andMers6922617
23andMe allrs6922617
SNP Nexus

SNPshotrs6922617
SNPdbers6922617
MSV3drs6922617
GWAS Ctlgrs6922617
GMAF0.101
Max Magnitude
? (A;A) (A;G) (G;G) 28
Linked to increased risk of Alzheimer's disease. [1]
GWAS snp
PMID [PMID 23562540OA-icon.png]
Trait Alzheimer's disease biomarkers
Title GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
Risk Allele A
P-val 4E-8
Odds Ratio .09 [NR] unit decrease