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rs4667682

From SNPedia

Orientationplus
Stabilizedplus
Make rs4667682(C;C)
Make rs4667682(C;T)
Make rs4667682(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position171271410
is asnp
is mentioned by
dbSNPrs4667682
ebirs4667682
HLIrs4667682
Exacrs4667682
Varsomers4667682
Maprs4667682
PheGenIrs4667682
hapmaprs4667682
1000 genomesrs4667682
hgdprs4667682
ensemblrs4667682
gopubmedrs4667682
geneviewrs4667682
scholarrs4667682
googlers4667682
pharmgkbrs4667682
gwascentralrs4667682
openSNPrs4667682
23andMers4667682
23andMe allrs4667682
SNP Nexus

SNPshotrs4667682
SNPdbers4667682
MSV3drs4667682
GWAS Ctlgrs4667682
GMAF0.225
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele C
P-val 0.000005
Odds Ratio None None