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rs10867752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10867752(C;T)
Make rs10867752(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position81400122
is asnp
is mentioned by
dbSNPrs10867752
ebirs10867752
HLIrs10867752
Exacrs10867752
Varsomers10867752
Maprs10867752
PheGenIrs10867752
hapmaprs10867752
1000 genomesrs10867752
hgdprs10867752
ensemblrs10867752
gopubmedrs10867752
geneviewrs10867752
scholarrs10867752
googlers10867752
pharmgkbrs10867752
gwascentralrs10867752
openSNPrs10867752
23andMers10867752
23andMe allrs10867752
SNP Nexus

SNPshotrs10867752
SNPdbers10867752
MSV3drs10867752
GWAS Ctlgrs10867752
GMAF0.08815
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000003
Odds Ratio NR NR


GET Evidence
rs10867752
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary