Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs721917
rs721917
0.740 GeneticVariation BEFREE Regarding rs721917, the T allele may increase the risk of chronic obstructive pulmonary disease</span> in the Asian population. 31116231

2019

dbSNP: rs721917
rs721917
0.740 GeneticVariation BEFREE Significant association of risk was also observed for "T" allele or "TT" genotype of rs721917 from SFTPD with COPD and AECOPD. 31057601

2019

dbSNP: rs721917
rs721917
G 0.740 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561

2019

dbSNP: rs721917
rs721917
G 0.740 GeneticVariation GWASCAT Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. 28166215

2017

dbSNP: rs721917
rs721917
0.740 GeneticVariation BEFREE We report for the first time that rs3088308 is an important factor influencing systemic SP-D levels and confirm the previous association of rs721917 to the risk of COPD and serum SP-D levels. 22846212

2012

dbSNP: rs721917
rs721917
0.740 GeneticVariation BEFREE In the NETT-NAS case-control analysis, four SFTPD SNPs were associated with susceptibility to COPD: rs2245121 (P = 0.01), rs911887 (P = 0.006), rs6413520 (P = 0.004), and rs721917 (P = 0.006). 20448057

2011