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rs6590322

From SNPedia

Orientationplus
Stabilizedplus
Make rs6590322(C;C)
Make rs6590322(C;T)
Make rs6590322(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position128336515
is asnp
is mentioned by
dbSNPrs6590322
ebirs6590322
HLIrs6590322
Exacrs6590322
Varsomers6590322
Maprs6590322
PheGenIrs6590322
hapmaprs6590322
1000 genomesrs6590322
hgdprs6590322
ensemblrs6590322
gopubmedrs6590322
geneviewrs6590322
scholarrs6590322
googlers6590322
pharmgkbrs6590322
gwascentralrs6590322
openSNPrs6590322
23andMers6590322
23andMe allrs6590322
SNP Nexus

SNPshotrs6590322
SNPdbers6590322
MSV3drs6590322
GWAS Ctlgrs6590322
GMAF0.4931
Max Magnitude
? (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 0.000009
Odds Ratio NR NR


GET Evidence
rs6590322
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary