rs7005606, NRG1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942 2016
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942 2016
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014