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rs6856768

From SNPedia

Orientationplus
Stabilizedplus
Make rs6856768(A;A)
Make rs6856768(A;G)
Make rs6856768(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position30466544
is asnp
is mentioned by
dbSNPrs6856768
dbSNP (classic)rs6856768
ClinGenrs6856768
ebirs6856768
HLIrs6856768
Exacrs6856768
Gnomadrs6856768
Varsomers6856768
LitVarrs6856768
Maprs6856768
PheGenIrs6856768
Biobankrs6856768
1000 genomesrs6856768
hgdprs6856768
ensemblrs6856768
geneviewrs6856768
scholarrs6856768
googlers6856768
pharmgkbrs6856768
gwascentralrs6856768
openSNPrs6856768
23andMers6856768
SNPshotrs6856768
SNPdbers6856768
MSV3drs6856768
GWAS Ctlgrs6856768
GMAF0.4858
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22832961OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease.
Risk Allele
P-val 0.000005
Odds Ratio 1.1800 None