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rs11848070

From SNPedia

Orientationplus
Stabilizedplus
Make rs11848070(A;A)
Make rs11848070(A;G)
Make rs11848070(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position71040884
GenePCNX
is asnp
is mentioned by
dbSNPrs11848070
ebirs11848070
HLIrs11848070
Exacrs11848070
Varsomers11848070
Maprs11848070
PheGenIrs11848070
hapmaprs11848070
1000 genomesrs11848070
hgdprs11848070
ensemblrs11848070
gopubmedrs11848070
geneviewrs11848070
scholarrs11848070
googlers11848070
pharmgkbrs11848070
gwascentralrs11848070
openSNPrs11848070
23andMers11848070
23andMe allrs11848070
SNP Nexus

SNPshotrs11848070
SNPdbers11848070
MSV3drs11848070
GWAS Ctlgrs11848070
GMAF0.123
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22881374OA-icon.png]
Trait Alzheimer's disease (late onset)
Title Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.
Risk Allele C
P-val 6E-6
Odds Ratio NR NR