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rs12570947

From SNPedia

Orientationplus
Stabilizedplus
Make rs12570947(C;C)
Make rs12570947(C;T)
Make rs12570947(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position107810092
is asnp
is mentioned by
dbSNPrs12570947
ebirs12570947
HLIrs12570947
Exacrs12570947
Varsomers12570947
Maprs12570947
PheGenIrs12570947
hapmaprs12570947
1000 genomesrs12570947
hgdprs12570947
ensemblrs12570947
gopubmedrs12570947
geneviewrs12570947
scholarrs12570947
googlers12570947
pharmgkbrs12570947
gwascentralrs12570947
openSNPrs12570947
23andMers12570947
23andMe allrs12570947
SNP Nexus

SNPshotrs12570947
SNPdbers12570947
MSV3drs12570947
GWAS Ctlgrs12570947
GMAF0.2672
Max Magnitude
? (C;C) (C;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 0.000004
Odds Ratio 1.4500 None