Have questions? Visit https://www.reddit.com/r/SNPedia

rs1031261

From SNPedia

Orientationminus
Stabilizedminus
Make rs1031261(C;C)
Make rs1031261(C;G)
Make rs1031261(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position32640454
GeneTTC27
is asnp
is mentioned by
dbSNPrs1031261
ebirs1031261
HLIrs1031261
Exacrs1031261
Varsomers1031261
Maprs1031261
PheGenIrs1031261
hapmaprs1031261
1000 genomesrs1031261
hgdprs1031261
ensemblrs1031261
gopubmedrs1031261
geneviewrs1031261
scholarrs1031261
googlers1031261
pharmgkbrs1031261
gwascentralrs1031261
openSNPrs1031261
23andMers1031261
23andMe allrs1031261
SNP Nexus

SNPshotrs1031261
SNPdbers1031261
MSV3drs1031261
GWAS Ctlgrs1031261
GMAF0.1635
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele C
P-val 0.000002
Odds Ratio None None