rs597668

Orientation

plus

Stabilized

plus

Make rs597668(C;C)

Make rs597668(C;T)

Make rs597668(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

45205630

is a	snp
is	mentioned by
dbSNP	rs597668
dbSNP (classic)	rs597668
ClinGen	rs597668
ebi	rs597668
HLI	rs597668
Exac	rs597668
Gnomad	rs597668
Varsome	rs597668
LitVar	rs597668
Map	rs597668
PheGenI	rs597668
Biobank	rs597668
1000 genomes	rs597668
hgdp	rs597668
ensembl	rs597668
geneview	rs597668
scholar	rs597668
google	rs597668
pharmgkb	rs597668
gwascentral	rs597668
openSNP	rs597668
23andMe	rs597668
SNPshot	rs597668
SNPdbe	rs597668
MSV3d	rs597668
GWAS Ctlg	rs597668

GMAF

0.2998

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 20460622] Genome-wide analysis of genetic loci associated with Alzheimer disease

[PMID 21321396] 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 21379329] 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.