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rs78647349

From SNPedia

Orientationplus
Stabilizedplus
Make rs78647349(A;A)
Make rs78647349(A;G)
Make rs78647349(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position5235426
GeneSTK32B
is asnp
is mentioned by
dbSNPrs78647349
ebirs78647349
HLIrs78647349
Exacrs78647349
Varsomers78647349
Maprs78647349
PheGenIrs78647349
hapmaprs78647349
1000 genomesrs78647349
hgdprs78647349
ensemblrs78647349
gopubmedrs78647349
geneviewrs78647349
scholarrs78647349
googlers78647349
pharmgkbrs78647349
gwascentralrs78647349
openSNPrs78647349
23andMers78647349
23andMe allrs78647349
SNP Nexus

SNPshotrs78647349
SNPdbers78647349
MSV3drs78647349
GWAS Ctlgrs78647349
GMAF0.04224
Max Magnitude
GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 5E-7
Odds Ratio .30 unit decrease