Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35705950
rs35705950
T 0.900 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs35705950
rs35705950
T 0.900 GeneticVariation GWASDB Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs35705950
rs35705950
T 0.900 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs2736100
rs2736100
A 0.840 GeneticVariation GWASCAT A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. 18835860

2008

dbSNP: rs2736100
rs2736100
A 0.840 GeneticVariation GWASDB A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. 18835860

2008

dbSNP: rs5743890
rs5743890
A 0.830 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs5743890
rs5743890
A 0.830 GeneticVariation GWASDB Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs17690703
rs17690703
C 0.800 GeneticVariation GWASDB Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs17690703
rs17690703
C 0.800 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs5743894
rs5743894
G 0.800 GeneticVariation GWASDB Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs5743894
rs5743894
G 0.800 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs121917737
rs121917737
0.800 GeneticVariation UNIPROT Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. 19100526

2009

dbSNP: rs121917738
rs121917738
0.800 GeneticVariation UNIPROT Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. 19100526

2009

dbSNP: rs121917737
rs121917737
A 0.800 CausalMutation CLINVAR

dbSNP: rs121917738
rs121917738
G 0.800 CausalMutation CLINVAR

dbSNP: rs2076295
rs2076295
DSP
G 0.730 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs62025270
rs62025270
A 0.710 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs28673968
rs28673968
T 0.700 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs73606754
rs73606754
C 0.700 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs146221660
rs146221660
A 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015

dbSNP: rs201540674
rs201540674
A 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015

dbSNP: rs398123017
rs398123017
T 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015

dbSNP: rs748223349
rs748223349
C 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015

dbSNP: rs776744306
rs776744306
C 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015

dbSNP: rs863225053
rs863225053
G 0.700 CausalMutation CLINVAR Rare variants in RTEL1 are associated with familial interstitial pneumonia. 25607374

2015