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rs10868366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(G;G) 0 average
(G;T) reduced risk for AD?
(T;T) reduced risk for AD?
ReferenceGRCh38 38.1/141
Chromosome9
Position86085145
GeneGOLM1
is asnp
is mentioned by
dbSNPrs10868366
ebirs10868366
HLIrs10868366
Exacrs10868366
Varsomers10868366
Maprs10868366
PheGenIrs10868366
hapmaprs10868366
1000 genomesrs10868366
hgdprs10868366
ensemblrs10868366
gopubmedrs10868366
geneviewrs10868366
scholarrs10868366
googlers10868366
pharmgkbrs10868366
gwascentralrs10868366
openSNPrs10868366
23andMers10868366
23andMe allrs10868366
SNP Nexus

SNPshotrs10868366
SNPdbers10868366
MSV3drs10868366
GWAS Ctlgrs10868366
GMAF0.3205
Max Magnitude0
? (G;G) (G;T) (T;T) 28
rs10868366, a SNP in the GOLM1 gene, is associated with reduced risk for Alzheimer's disease in a study of ~1100 Canadian patients. The protective allele appears to be rs10868366(T), giving an odds ratio of 0.55 (CI: 0.40 - 0.75). [PMID 17998437]


[PMID 20570408] Genetic variation in GOLM1 and prefrontal cortical volume in Alzheimer's disease

[PMID 19749441] GOLPH2 gene markers are not associated with Alzheimer's disease in a sample of the Spanish population.

[PMID 20574532OA-icon.png] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.

[PMID 22167654] Association studies of 19 candidate SNPs with sporadic Alzheimer's disease in the North Chinese Han population.