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

rs6107516

From SNPedia

Orientationplus
Stabilizedplus
Make rs6107516(A;A)
Make rs6107516(A;G)
Make rs6107516(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position4696446
GenePRNP
is asnp
is mentioned by
dbSNPrs6107516
ebirs6107516
HLIrs6107516
Exacrs6107516
Varsomers6107516
Maprs6107516
PheGenIrs6107516
hapmaprs6107516
1000 genomesrs6107516
hgdprs6107516
ensemblrs6107516
gopubmedrs6107516
geneviewrs6107516
scholarrs6107516
googlers6107516
pharmgkbrs6107516
gwascentralrs6107516
openSNPrs6107516
23andMers6107516
23andMe allrs6107516
SNP Nexus

SNPshotrs6107516
SNPdbers6107516
MSV3drs6107516
GWAS Ctlgrs6107516
GMAF0.1869
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22137330]
Trait
Title Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Risk Allele
P-val 3E-18
Odds Ratio None None


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