SNP information rs17293632
Normal allele: CC
Polymorphism rs17293632 is related to topics like this:
A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...
Research and publications:
22396665 Interpreting meta-analyses of genome-wide association studies.
23028907 Limited evidence for parent-of-origin effects in inflammatory bowel disease associated loci.
26157023 Strategies for fine-mapping complex traits.
27156530 Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.
27386823 Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.
29300379 The role of SMAD3 in the genetic predisposition to papillary thyroid carcinoma.
29988570 GWAS Reveal Targets in Vessel Wall Pathways to Treat Coronary Artery Disease.
30065929 Integrating Genes Affecting Coronary Artery Disease in Functional Networks by Multi-OMICs Approach.
31043074 Genetic Insights Into Smooth Muscle Cell Contributions to Coronary Artery Disease.
24121259 Impact of CTGF single nucleotide polymorphisms on Crohn's disease outcomes.
Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...
Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...
Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...