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rs17767225

From SNPedia

Orientationplus
Stabilizedplus
Make rs17767225(C;C)
Make rs17767225(C;T)
Make rs17767225(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position71199580
is asnp
is mentioned by
dbSNPrs17767225
ebirs17767225
HLIrs17767225
Exacrs17767225
Varsomers17767225
Maprs17767225
PheGenIrs17767225
hapmaprs17767225
1000 genomesrs17767225
hgdprs17767225
ensemblrs17767225
gopubmedrs17767225
geneviewrs17767225
scholarrs17767225
googlers17767225
pharmgkbrs17767225
gwascentralrs17767225
openSNPrs17767225
23andMers17767225
23andMe allrs17767225
SNP Nexus

SNPshotrs17767225
SNPdbers17767225
MSV3drs17767225
GWAS Ctlgrs17767225
GMAF0.07943
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 8E-6
Odds Ratio NR NR