Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7671167
rs7671167
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		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
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		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
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		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
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		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
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.840 GeneticVariation GWASDB Identification of FGF7 as a novel susceptibility locus for chronic obstructive pulmonary disease. 21921092 2011
dbSNP: rs7671167
rs7671167
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.840 GeneticVariation GWASDB Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748 2010
dbSNP: rs7671167
rs7671167
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.840 GeneticVariation GWASCAT Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748 2010
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.820 GeneticVariation BEFREE The FAM13A rs2869967 was associated with COPD (minor CC genotype: P = 0.0007, OR = 2.414). 26310313 2015
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		C 0.820 GeneticVariation GWASCAT Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. 25241909 2014
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.820 GeneticVariation BEFREE Significant differences in genotypic distributions (χ(2)=6.319, p=0.042 for rs2869967</span>; χ(2)=6.062, p=0.048 for rs3821104) and allele distributions (χ(2)=4.014, p=0.045 for rs2869967; χ(2)=5.607, p=0.018 for rs3821104) were observed between patients and control subjects for variants rs2869967 and rs3821104, whereas no statistically significant associations for genotypic and allelic distribution between IREB2 rs2568494 and COPD phenotype (p>0.05) were identified. 22027142 2011
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.820 GeneticVariation GWASDB Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748 2010
dbSNP: rs3822072
rs3822072
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0392885
Disease:
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs3822072
rs3822072
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs2609255
rs2609255
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013
dbSNP: rs2609255
rs2609255
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013
dbSNP: rs3822072
rs3822072
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs3822072
rs3822072
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs1964516
rs1964516
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.800 GeneticVariation GWASDB A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. 22080838 2012
dbSNP: rs1964516
rs1964516
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.800 GeneticVariation GWASCAT A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. 22080838 2012
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0016529
Disease:
Forced expiratory volume function 		0.800 GeneticVariation GWASDB Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. 23284291 2012
dbSNP: rs1903003
rs1903003
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.710 GeneticVariation BEFREE The rs1903003, rs7671167 FAM13A variants confer a protective effect on COPD (both P < 0.002, OR < 0.405). 26310313 2015
dbSNP: rs1903003
rs1903003
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.710 GeneticVariation GWASDB Identification of FGF7 as a novel susceptibility locus for chronic obstructive pulmonary disease. 21921092 2011
dbSNP: rs1903003
rs1903003
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.710 GeneticVariation GWASDB Variants in FAM13A are associated with chronic obstructive pulmonary disease. 20173748 2010
dbSNP: rs2167750
rs2167750
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019