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rs4845552

From SNPedia

Orientationplus
Stabilizedplus
Make rs4845552(A;A)
Make rs4845552(A;G)
Make rs4845552(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position153507522
is asnp
is mentioned by
dbSNPrs4845552
ebirs4845552
HLIrs4845552
Exacrs4845552
Varsomers4845552
Maprs4845552
PheGenIrs4845552
hapmaprs4845552
1000 genomesrs4845552
hgdprs4845552
ensemblrs4845552
gopubmedrs4845552
geneviewrs4845552
scholarrs4845552
googlers4845552
pharmgkbrs4845552
gwascentralrs4845552
openSNPrs4845552
23andMers4845552
23andMe allrs4845552
SNP Nexus

SNPshotrs4845552
SNPdbers4845552
MSV3drs4845552
GWAS Ctlgrs4845552
GMAF0.1272
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio NR NR


GET Evidence
rs4845552
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.898438
summary