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rs10784496

From SNPedia

Orientationplus
Stabilizedplus
Make rs10784496(A;A)
Make rs10784496(A;G)
Make rs10784496(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position65767191
GeneRPSAP52
is asnp
is mentioned by
dbSNPrs10784496
dbSNP (classic)rs10784496
ClinGenrs10784496
ebirs10784496
HLIrs10784496
Exacrs10784496
Gnomadrs10784496
Varsomers10784496
LitVarrs10784496
Maprs10784496
PheGenIrs10784496
Biobankrs10784496
1000 genomesrs10784496
hgdprs10784496
ensemblrs10784496
geneviewrs10784496
scholarrs10784496
googlers10784496
pharmgkbrs10784496
gwascentralrs10784496
openSNPrs10784496
23andMers10784496
SNPshotrs10784496
SNPdbers10784496
MSV3drs10784496
GWAS Ctlgrs10784496
GMAF0.3939
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20932310OA-icon.png]
Trait
Title Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study
Risk Allele G
P-val 3E-7
Odds Ratio None None