Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2787094
rs2787094
Entrez Id: 80332
Gene Symbol: ADAM33
ADAM33
CUI: C0861155
Disease:
Rhinoconjunctivitis
0.010 GeneticVariation BEFREE The GC genotype of rs2787094, the CT genotype of rs628977, and the haplotype containing the rs2787094 C allele, the rs628977 T allele, the rs2853209 T allele, and the rs612709 G allele were significantly inversely associated with rhinoconjunctivitis. 22349453 2012