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rs10850408

From SNPedia

Orientationplus
Stabilizedplus
Make rs10850408(C;C)
Make rs10850408(C;T)
Make rs10850408(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position114942588
is asnp
is mentioned by
dbSNPrs10850408
ebirs10850408
HLIrs10850408
Exacrs10850408
Varsomers10850408
Maprs10850408
PheGenIrs10850408
hapmaprs10850408
1000 genomesrs10850408
hgdprs10850408
ensemblrs10850408
gopubmedrs10850408
geneviewrs10850408
scholarrs10850408
googlers10850408
pharmgkbrs10850408
gwascentralrs10850408
openSNPrs10850408
23andMers10850408
23andMe allrs10850408
SNP Nexus

SNPshotrs10850408
SNPdbers10850408
MSV3drs10850408
GWAS Ctlgrs10850408
GMAF0.2649
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22159054OA-icon.png]
Trait
Title A comprehensive genetic association study of Alzheimer disease in African Americans.
Risk Allele
P-val 9E-7
Odds Ratio 1.5900 None