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rs1018361

From SNPedia

Orientationplus
Stabilizedplus
Make rs1018361(C;C)
Make rs1018361(C;T)
Make rs1018361(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203820112
is asnp
is mentioned by
dbSNPrs1018361
ebirs1018361
HLIrs1018361
Exacrs1018361
Varsomers1018361
Maprs1018361
PheGenIrs1018361
hapmaprs1018361
1000 genomesrs1018361
hgdprs1018361
ensemblrs1018361
gopubmedrs1018361
geneviewrs1018361
scholarrs1018361
googlers1018361
pharmgkbrs1018361
gwascentralrs1018361
openSNPrs1018361
23andMers1018361
23andMe allrs1018361
SNP Nexus

SNPshotrs1018361
SNPdbers1018361
MSV3drs1018361
GWAS Ctlgrs1018361
GMAF0.2888
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20017994OA-icon.png] Pathway-based analysis of a genome-wide case-control association study of rheumatoid arthritis


[PMID 20017967OA-icon.png] Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results.