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rs11190141

From SNPedia

Orientationplus
Stabilizedplus
Make rs11190141(C;C)
Make rs11190141(C;T)
Make rs11190141(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position99532633
GeneNKX2-3
is asnp
is mentioned by
dbSNPrs11190141
ebirs11190141
HLIrs11190141
Exacrs11190141
Varsomers11190141
Maprs11190141
PheGenIrs11190141
hapmaprs11190141
1000 genomesrs11190141
hgdprs11190141
ensemblrs11190141
gopubmedrs11190141
geneviewrs11190141
scholarrs11190141
googlers11190141
pharmgkbrs11190141
gwascentralrs11190141
openSNPrs11190141
23andMers11190141
23andMe allrs11190141
SNP Nexus

SNPshotrs11190141
SNPdbers11190141
MSV3drs11190141
GWAS Ctlgrs11190141
GMAF0.4275
Max Magnitude
GWAS snp
PMID [PMID 22412388OA-icon.png]
Trait
Title A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
Risk Allele C
P-val 5E-7
Odds Ratio 1.3400 None