Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation BEFREE Our results were the first time to reveal that SNPs from FAM13A (rs7671167), SETD7 (rs17050782), and a haplotype of VEGFA ("GGCGC") are potential susceptibility loci associated with increased COPD risk in Chinese Li minority population. 26251585

2015
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation BEFREE The rs1903003, rs7671167 FAM13A variants confer a protective effect on COPD (both P < 0.002, OR < 0.405). 26310313

2015
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation BEFREE Statistical analysis revealed that SNP rs7671167 was associated with COPD in former smokers with adjusted P-value of 0.026. 23891779

2013
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation BEFREE We included three SNPs previously associated with COPD: rs7671167 (FAM13A), rs13180 (IREB2), and rs8034191 (CHRNA 3/5), and four SNPs associated with lung function in a genome-wide association study of general population samples: rs2070600 (AGER), rs11134242 (ADCY2), rs4316710 (THSD4), and rs17096090 (INTS12). 22461431

2012
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation GWASDB Identification of FGF7 as a novel susceptibility locus for chronic obstructive pulmonary disease. 21921092

2011
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation GWASDB Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748

2010
dbSNP: rs7671167
rs7671167
FAM13A
0.840 GeneticVariation GWASCAT Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748

2010