Have questions? Visit https://www.reddit.com/r/SNPedia

rs597668

From SNPedia

Orientationplus
Stabilizedplus
Make rs597668(C;C)
Make rs597668(C;T)
Make rs597668(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position45205630
is asnp
is mentioned by
dbSNPrs597668
ebirs597668
HLIrs597668
Exacrs597668
Varsomers597668
Maprs597668
PheGenIrs597668
hapmaprs597668
1000 genomesrs597668
hgdprs597668
ensemblrs597668
gopubmedrs597668
geneviewrs597668
scholarrs597668
googlers597668
pharmgkbrs597668
gwascentralrs597668
openSNPrs597668
23andMers597668
23andMe allrs597668
SNP Nexus

SNPshotrs597668
SNPdbers597668
MSV3drs597668
GWAS Ctlgrs597668
GMAF0.2998
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20460622OA-icon.png] Genome-wide analysis of genetic loci associated with Alzheimer disease


[PMID 21321396OA-icon.png] Replication of BIN1 Association with Alzheimer's Disease and Evaluation of Genetic Interactions


[PMID 21220176] Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.


[PMID 21379329OA-icon.png] Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.


[PMID 22381399] Lack of association between rs597668 polymorphism near EXOC3L2 and late-onset Alzheimer's disease in Han Chinese.


[PMID 23663385] Association between EXOC3L2 rs597668 polymorphism and Alzheimer's disease.


[PMID 26680604] Polygenic Analysis of Late-Onset Alzheimer's Disease from Mainland China.