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rs4773460

From SNPedia

Orientationplus
Stabilizedplus
Make rs4773460(C;C)
Make rs4773460(C;T)
Make rs4773460(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position86590602
is asnp
is mentioned by
dbSNPrs4773460
ebirs4773460
HLIrs4773460
Exacrs4773460
Varsomers4773460
Maprs4773460
PheGenIrs4773460
hapmaprs4773460
1000 genomesrs4773460
hgdprs4773460
ensemblrs4773460
gopubmedrs4773460
geneviewrs4773460
scholarrs4773460
googlers4773460
pharmgkbrs4773460
gwascentralrs4773460
openSNPrs4773460
23andMers4773460
23andMe allrs4773460
SNP Nexus

SNPshotrs4773460
SNPdbers4773460
MSV3drs4773460
GWAS Ctlgrs4773460
GMAF0.2167
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 0.000002
Odds Ratio NR NR


GET Evidence
rs4773460
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary