rs1800897, PAX2

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
0.010 GeneticVariation BEFREE The PAX2 heterozygous genotype 798C>T did not increase susceptibility to H</span>SP, however, it may be used clinically as a screening indicator for HSP in children with a high risk of renal involvement. 25385517 2015
Nephritis
CUI: C0027697
Disease: Nephritis
0.010 GeneticVariation BEFREE However, the frequency of the PAX2 heterozygous genotype 798C>T in the HSP with nephritis (HSPN) group was significantly higher than those in the controls and in the HSP without nephritis group (P<0.05). 25385517 2015