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rs1029273

From SNPedia

Orientationplus
Stabilizedplus
Make rs1029273(C;C)
Make rs1029273(C;T)
Make rs1029273(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4675114
is asnp
is mentioned by
dbSNPrs1029273
ebirs1029273
HLIrs1029273
Exacrs1029273
Varsomers1029273
Maprs1029273
PheGenIrs1029273
hapmaprs1029273
1000 genomesrs1029273
hgdprs1029273
ensemblrs1029273
gopubmedrs1029273
geneviewrs1029273
scholarrs1029273
googlers1029273
pharmgkbrs1029273
gwascentralrs1029273
openSNPrs1029273
23andMers1029273
23andMe allrs1029273
SNP Nexus

SNPshotrs1029273
SNPdbers1029273
MSV3drs1029273
GWAS Ctlgrs1029273
GMAF0.4279
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21616973] Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors


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