Have questions? Visit https://www.reddit.com/r/SNPedia

rs12474609

From SNPedia

Orientationplus
Stabilizedplus
Make rs12474609(A;A)
Make rs12474609(A;T)
Make rs12474609(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position140963573
GeneLRP1B
is asnp
is mentioned by
dbSNPrs12474609
ebirs12474609
HLIrs12474609
Exacrs12474609
Varsomers12474609
Maprs12474609
PheGenIrs12474609
hapmaprs12474609
1000 genomesrs12474609
hgdprs12474609
ensemblrs12474609
gopubmedrs12474609
geneviewrs12474609
scholarrs12474609
googlers12474609
pharmgkbrs12474609
gwascentralrs12474609
openSNPrs12474609
23andMers12474609
23andMe allrs12474609
SNP Nexus

SNPshotrs12474609
SNPdbers12474609
MSV3drs12474609
GWAS Ctlgrs12474609
GMAF0.213
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 19367585]
Trait Successful cognitive aging
Title A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis
Risk Allele
P-val 6E-9
Odds Ratio



GET Evidence
rs12474609
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.106383
summary