Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 3084
Gene Symbol: NRG1
NRG1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.500 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 2674
Gene Symbol: GFRA1
GFRA1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.370 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 55454
Gene Symbol: CSGALNACT2
CSGALNACT2
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.110 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 221002
Gene Symbol: RASGEF1A
RASGEF1A
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.110 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 3802
Gene Symbol: KIR2DL1
KIR2DL1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 100506697
Gene Symbol: LINC00327
LINC00327
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 3806
Gene Symbol: KIR2DS1
KIR2DS1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 3811
Gene Symbol: KIR3DL1
KIR3DL1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 23504
Gene Symbol: RIMBP2
RIMBP2
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 84696
Gene Symbol: ABHD1
ABHD1
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
Entrez Id: 3809
Gene Symbol: KIR2DS4
KIR2DS4
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.100 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009