Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1903003
rs1903003
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. 22797724 2012
dbSNP: rs2869966
rs2869966
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0005823
Disease:
Blood Pressure 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs3822072
rs3822072
Entrez Id: 10144
Gene Symbol: FAM13A
FAM13A
CUI: C0005893
Disease:
Body mass index procedure 		0.700 GeneticVariation GWASDB Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. 22885924 2012
dbSNP: rs1059122
rs1059122
Entrez Id: 10144;285512
Gene Symbol: FAM13A;FAM13A-AS1
FAM13A;FAM13A-AS1
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE Our results suggested that rs1059122 (FAM13A), rs17748 (PHLDB1), and rs4809957 (CYP24A1) might contribute to breast cancer susceptibility in the Chinese Han population. 31215377 2019
dbSNP: rs2869967
rs2869967
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0008677
Disease:
Bronchitis, Chronic 		C 0.700 GeneticVariation GWASCAT Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. 25241909 2014
dbSNP: rs4416442
rs4416442
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0008677
Disease:
Bronchitis, Chronic 		0.700 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: C0684249
Disease:
Carcinoma of lung 		0.010 GeneticVariation BEFREE We examined IREB2 variants (rs2568494, rs2656069, rs10851906, rs13180) and FAM13A (rs1903003, rs7671167, rs2869967) among 1.141 participants (468 LC, 149 COPD, 524 smoking controls). 26310313 2015
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 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 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 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 GWASCAT 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 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 BEFREE The rs1903003, rs7671167 FAM13A variants confer a protective effect on COPD (both P < 0.002, OR < 0.405). 26310313 2015
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: 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 BEFREE The FAM13A rs2869967 was associated with COPD (minor CC genotype: P = 0.0007, OR = 2.414). 26310313 2015
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: 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: 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: rs2869966
rs2869966
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		T 0.700 GeneticVariation GWASCAT Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. 25241909 2014
dbSNP: rs2869966
rs2869966
Entrez Id: 10144;105377327
Gene Symbol: FAM13A;LOC105377327
FAM13A;LOC105377327
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019