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rs10793294

From SNPedia

Orientationplus
Stabilizedplus
Make rs10793294(A;A)
Make rs10793294(A;C)
Make rs10793294(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position78285357
GeneGAB2
is asnp
is mentioned by
dbSNPrs10793294
ebirs10793294
HLIrs10793294
Exacrs10793294
Varsomers10793294
Maprs10793294
PheGenIrs10793294
hapmaprs10793294
1000 genomesrs10793294
hgdprs10793294
ensemblrs10793294
gopubmedrs10793294
geneviewrs10793294
scholarrs10793294
googlers10793294
pharmgkbrs10793294
gwascentralrs10793294
openSNPrs10793294
23andMers10793294
23andMe allrs10793294
SNP Nexus

SNPshotrs10793294
SNPdbers10793294
MSV3drs10793294
GWAS Ctlgrs10793294
GMAF0.4876
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 21108942] Common variant in GRB2 is associated with late-onset Alzheimer's disease in Han Chinese

[PMID 17553421OA-icon.png] GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.


[PMID 23071633OA-icon.png] Mining pure, strict epistatic interactions from high-dimensional datasets: ameliorating the curse of dimensionality.