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rs6116492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs6116492(G;T)
Make rs6116492(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4717980
is asnp
is mentioned by
dbSNPrs6116492
ebirs6116492
HLIrs6116492
Exacrs6116492
Varsomers6116492
Maprs6116492
PheGenIrs6116492
hapmaprs6116492
1000 genomesrs6116492
hgdprs6116492
ensemblrs6116492
gopubmedrs6116492
geneviewrs6116492
scholarrs6116492
googlers6116492
pharmgkbrs6116492
gwascentralrs6116492
openSNPrs6116492
23andMers6116492
23andMe allrs6116492
SNP Nexus

SNPshotrs6116492
SNPdbers6116492
MSV3drs6116492
GWAS Ctlgrs6116492
GMAF0.06612
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22137330]
Trait
Title Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Risk Allele
P-val 5E-7
Odds Ratio None None


[PMID 19081515OA-icon.png] Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.