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rs1460163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1460163(A;A)
Make rs1460163(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position79315213
is asnp
is mentioned by
dbSNPrs1460163
ebirs1460163
HLIrs1460163
Exacrs1460163
Varsomers1460163
Maprs1460163
PheGenIrs1460163
hapmaprs1460163
1000 genomesrs1460163
hgdprs1460163
ensemblrs1460163
gopubmedrs1460163
geneviewrs1460163
scholarrs1460163
googlers1460163
pharmgkbrs1460163
gwascentralrs1460163
openSNPrs1460163
23andMers1460163
23andMe allrs1460163
SNP Nexus

SNPshotrs1460163
SNPdbers1460163
MSV3drs1460163
GWAS Ctlgrs1460163
GMAF0.2466
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19081515OA-icon.png]
Trait Creutzfeldt-Jakob disease
Title Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study
Risk Allele A
P-val 6E-8
Odds Ratio NR NR



GET Evidence
rs1460163
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary