rs8182352, None

N. diseases: 5
Disease: Hamman-Rich syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
0.010 GeneticVariation BEFREE Conditional analyses revealed a significant association for the NLRP1 rs8182352 variant with both anti-topoisomerase-positive and SSc-related fibrosing alveolitis (FA) subsets under an additive model: p=0.0042, OR 1.23 (95% CI 1.07 to 1.41) and p=0.0065 OR 1.19 (95% CI 1.05 to 1.36), respectively. 21149496 2011