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rs10792830

From SNPedia

Orientationplus
Stabilizedplus
Make rs10792830(A;A)
Make rs10792830(A;G)
Make rs10792830(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position86127766
is asnp
is mentioned by
dbSNPrs10792830
dbSNP (classic)rs10792830
ClinGenrs10792830
ebirs10792830
HLIrs10792830
Exacrs10792830
Gnomadrs10792830
Varsomers10792830
LitVarrs10792830
Maprs10792830
PheGenIrs10792830
Biobankrs10792830
1000 genomesrs10792830
hgdprs10792830
ensemblrs10792830
geneviewrs10792830
scholarrs10792830
googlers10792830
pharmgkbrs10792830
gwascentralrs10792830
openSNPrs10792830
23andMers10792830
SNPshotrs10792830
SNPdbers10792830
MSV3drs10792830
GWAS Ctlgrs10792830
GMAF0.4706
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000006
Odds Ratio 1.2500 None