Disease: Hirschsprung Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs671600
rs671600
Entrez Id: 3802;3806;3809;3811
Gene Symbol: KIR2DL1;KIR2DS1;KIR2DS4;KIR3DL1
KIR2DL1;KIR2DS1;KIR2DS4;KIR3DL1
CUI: C0019569
Disease:
Hirschsprung Disease 		0.700 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009