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rs1819658

From SNPedia

Orientationplus
Stabilizedplus
Make rs1819658(C;C)
Make rs1819658(C;T)
Make rs1819658(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position58153390
is asnp
is mentioned by
dbSNPrs1819658
ebirs1819658
HLIrs1819658
Exacrs1819658
Varsomers1819658
Maprs1819658
PheGenIrs1819658
hapmaprs1819658
1000 genomesrs1819658
hgdprs1819658
ensemblrs1819658
gopubmedrs1819658
geneviewrs1819658
scholarrs1819658
googlers1819658
pharmgkbrs1819658
gwascentralrs1819658
openSNPrs1819658
23andMers1819658
23andMe allrs1819658
SNP Nexus

SNPshotrs1819658
SNPdbers1819658
MSV3drs1819658
GWAS Ctlgrs1819658
GMAF0.3287
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele C
P-val 9E-17
Odds Ratio 1.1900 [1.13-1.25]