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

rs17293632

From SNPedia

Orientationplus
Stabilizedplus
Make rs17293632(C;C)
Make rs17293632(C;T)
Make rs17293632(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position67150258
GeneSMAD3
is asnp
is mentioned by
dbSNPrs17293632
ebirs17293632
HLIrs17293632
Exacrs17293632
Varsomers17293632
Maprs17293632
PheGenIrs17293632
hapmaprs17293632
1000 genomesrs17293632
hgdprs17293632
ensemblrs17293632
gopubmedrs17293632
geneviewrs17293632
scholarrs17293632
googlers17293632
pharmgkbrs17293632
gwascentralrs17293632
openSNPrs17293632
23andMers17293632
23andMe allrs17293632
SNP Nexus

SNPshotrs17293632
SNPdbers17293632
MSV3drs17293632
GWAS Ctlgrs17293632
GMAF0.1079
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 T
P-val 3E-19
Odds Ratio 1.1200 [1.07-1.16]
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Inflammatory bowel disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele T
P-val 6E-16
Odds Ratio 1.07 [1.032-1.102]


[PMID 24121259] The Influence of CTGF Single-Nucleotide Polymorphisms on Outcomes in Crohn's Disease