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rs12989701

From SNPedia

Orientationplus
Stabilizedplus
Make rs12989701(A;A)
Make rs12989701(A;C)
Make rs12989701(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position127130409
is asnp
is mentioned by
dbSNPrs12989701
ebirs12989701
HLIrs12989701
Exacrs12989701
Varsomers12989701
Maprs12989701
PheGenIrs12989701
hapmaprs12989701
1000 genomesrs12989701
hgdprs12989701
ensemblrs12989701
gopubmedrs12989701
geneviewrs12989701
scholarrs12989701
googlers12989701
pharmgkbrs12989701
gwascentralrs12989701
openSNPrs12989701
23andMers12989701
23andMe allrs12989701
SNP Nexus

SNPshotrs12989701
SNPdbers12989701
MSV3drs12989701
GWAS Ctlgrs12989701
GMAF0.09045
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21390209OA-icon.png]
Trait
Title Meta-Analysis for Genome-Wide Association Study Identifies Multiple Variants at the BIN1 Locus Associated with Late-Onset Alzheimer's Disease
Risk Allele
P-val 3E-10
Odds Ratio 1.2300 [NR]