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rs990324

From SNPedia

Orientationplus
Stabilizedplus
Make rs990324(A;A)
Make rs990324(A;G)
Make rs990324(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32813108
GeneLINC00423
is asnp
is mentioned by
dbSNPrs990324
ebirs990324
HLIrs990324
Exacrs990324
Varsomers990324
Maprs990324
PheGenIrs990324
hapmaprs990324
1000 genomesrs990324
hgdprs990324
ensemblrs990324
gopubmedrs990324
geneviewrs990324
scholarrs990324
googlers990324
pharmgkbrs990324
gwascentralrs990324
openSNPrs990324
23andMers990324
23andMe allrs990324
SNP Nexus

SNPshotrs990324
SNPdbers990324
MSV3drs990324
GWAS Ctlgrs990324
GMAF0.1699
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000005
Odds Ratio 0.0064 [NR] unit decrease (interaction)