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Pulmonary fibrosis

From SNPedia


Pulmonary fibrosis is a condition in which the tissue deep in lungs becomes scarred over time.

Publications[edit]

[PMID 29653950OA-icon.png] Personalised medicine in interstitial lung diseases: Number 6 in the Series "Personalised medicine in respiratory diseases" Edited by Renaud Louis and Nicolas Roche.

[PMID 29066090OA-icon.png] Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.

[PMID 28166215OA-icon.png] Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.

[PMID 27799632OA-icon.png] Pulmonary fibrosis in the era of stratified medicine.

[PMID 26893575OA-icon.png] Candidate genes of idiopathic pulmonary fibrosis: current evidence and research.

[PMID 23583980OA-icon.png] Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

[PMID 22802285OA-icon.png] The genetic and environmental causes of pulmonary fibrosis.

[PMID 18835860] A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.

Associated SNPs and genes[edit]

SNPs[edit]

rs1278769

rs1981997

rs2034650

rs2076295

rs2296160

rs2609255

rs2736100

rs2744371

rs3737002

rs4727443

rs5743890

rs5743894

rs6793295

rs7144383

rs7574865

rs7934606

rs11191865

rs12610495

rs12951053

rs17690703

rs28673968

rs34094720

rs35705950

rs62025270

rs73606754

rs117791180

rs191031841

Genes[edit]

ATP11A

DPP9

DSP

FAM13A

GOSR2

LOC101929679

LOC105377329

MAPT-AS1

MDGA2

MUC5AC

MUC5B

OBFC1

SRD5A2

TERC

TERT

TOLLIP

TTYH1