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rs12761224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12761224(G;T)
Make rs12761224(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position70767761
is asnp
is mentioned by
dbSNPrs12761224
ebirs12761224
HLIrs12761224
Exacrs12761224
Varsomers12761224
Maprs12761224
PheGenIrs12761224
hapmaprs12761224
1000 genomesrs12761224
hgdprs12761224
ensemblrs12761224
gopubmedrs12761224
geneviewrs12761224
scholarrs12761224
googlers12761224
pharmgkbrs12761224
gwascentralrs12761224
openSNPrs12761224
23andMers12761224
23andMe allrs12761224
SNP Nexus

SNPshotrs12761224
SNPdbers12761224
MSV3drs12761224
GWAS Ctlgrs12761224
GMAF0.07713
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22210626OA-icon.png]
Trait
Title Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Risk Allele
P-val 0.000006
Odds Ratio 1.3861 None