Have questions? Visit https://www.reddit.com/r/SNPedia

rs6478106

From SNPedia

Orientationplus
Stabilizedplus
Make rs6478106(C;C)
Make rs6478106(C;T)
Make rs6478106(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position114783386
GeneTNFSF15
is asnp
is mentioned by
dbSNPrs6478106
ebirs6478106
HLIrs6478106
Exacrs6478106
Varsomers6478106
Maprs6478106
PheGenIrs6478106
hapmaprs6478106
1000 genomesrs6478106
hgdprs6478106
ensemblrs6478106
gopubmedrs6478106
geneviewrs6478106
scholarrs6478106
googlers6478106
pharmgkbrs6478106
gwascentralrs6478106
openSNPrs6478106
23andMers6478106
23andMe allrs6478106
SNP Nexus

SNPshotrs6478106
SNPdbers6478106
MSV3drs6478106
GWAS Ctlgrs6478106
GMAF0.36
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele T
P-val 5E-46
Odds Ratio 1.73 [1.60-1.86]


[PMID 27647972] A case-control study about the association between vascular endothelial growth inhibitor gene polymorphisms and breast cancer risk in female patients in Northeast China.