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

rs11610206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs11610206(C;C)
Make rs11610206(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position47245743
is asnp
is mentioned by
dbSNPrs11610206
ebirs11610206
HLIrs11610206
Exacrs11610206
Varsomers11610206
Maprs11610206
PheGenIrs11610206
hapmaprs11610206
1000 genomesrs11610206
hgdprs11610206
ensemblrs11610206
gopubmedrs11610206
geneviewrs11610206
scholarrs11610206
googlers11610206
pharmgkbrs11610206
gwascentralrs11610206
openSNPrs11610206
23andMers11610206
23andMe allrs11610206
SNP Nexus

SNPshotrs11610206
SNPdbers11610206
MSV3drs11610206
GWAS Ctlgrs11610206
GMAF0.1065
Max Magnitude0
? (C;C) (C;T) (T;T) 28

news Alzheimer's disease

GWAS snp
PMID [PMID 19118814OA-icon.png]
Trait Alzheimer's disease
Title Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
Risk Allele
P-val 3E-7
Odds Ratio NR NR



[PMID 20883677] Genetic association of rs11610206 SNP on chromosome 12q13 with late-onset Alzheimer's disease in a Han Chinese population



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


GET Evidence
rs11610206
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary