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rs9871760

From SNPedia

Orientationplus
Stabilizedplus
Make rs9871760(A;A)
Make rs9871760(A;C)
Make rs9871760(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position127274256
is asnp
is mentioned by
dbSNPrs9871760
ebirs9871760
HLIrs9871760
Exacrs9871760
Varsomers9871760
Maprs9871760
PheGenIrs9871760
hapmaprs9871760
1000 genomesrs9871760
hgdprs9871760
ensemblrs9871760
gopubmedrs9871760
geneviewrs9871760
scholarrs9871760
googlers9871760
pharmgkbrs9871760
gwascentralrs9871760
openSNPrs9871760
23andMers9871760
23andMe allrs9871760
SNP Nexus

SNPshotrs9871760
SNPdbers9871760
MSV3drs9871760
GWAS Ctlgrs9871760
GMAF0.3765
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21116278]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000004
Odds Ratio 0.0074 [NR] unit decrease (main effect)