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rs13204742

From SNPedia

Orientationplus
Stabilizedplus
Make rs13204742(G;G)
Make rs13204742(G;T)
Make rs13204742(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position127924620
is asnp
is mentioned by
dbSNPrs13204742
ebirs13204742
HLIrs13204742
Exacrs13204742
Varsomers13204742
Maprs13204742
PheGenIrs13204742
hapmaprs13204742
1000 genomesrs13204742
hgdprs13204742
ensemblrs13204742
gopubmedrs13204742
geneviewrs13204742
scholarrs13204742
googlers13204742
pharmgkbrs13204742
gwascentralrs13204742
openSNPrs13204742
23andMers13204742
23andMe allrs13204742
SNP Nexus

SNPshotrs13204742
SNPdbers13204742
MSV3drs13204742
GWAS Ctlgrs13204742
GMAF0.06382
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele T
P-val 8E-15
Odds Ratio 1.17 [1.118-1.23]


[PMID 27438997] Increased THEMIS First Exon Usage in CD4+ T-Cells Is Associated with a Genotype that Is Protective against Multiple Sclerosis.