STN1, STN1 subunit of CST complex, 79991

N. diseases: 82; N. variants: 19
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11191865
rs11191865
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013
dbSNP: rs11191865
rs11191865
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013
dbSNP: rs1057519583
rs1057519583
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C4479220
Disease:
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2 		0.800 GeneticVariation UNIPROT
dbSNP: rs1057519583
rs1057519583
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C4479220
Disease:
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2 		G 0.800 CausalMutation CLINVAR
dbSNP: rs765462548
rs765462548
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C4479220
Disease:
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2 		A 0.800 CausalMutation CLINVAR
dbSNP: rs765462548
rs765462548
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C4479220
Disease:
CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2 		0.800 GeneticVariation UNIPROT
dbSNP: rs10786774
rs10786774
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10883944
rs10883944
Entrez Id: 79991
Gene Symbol: STN1
STN1
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
dbSNP: rs10883944
rs10883944
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C1821417
Disease:
RESTING HEART RATE 		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: rs11191841
rs11191841
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11191841
rs11191841
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C1518922
Disease:
peak expiratory flow (procedure) 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11191841
rs11191841
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11191841
rs11191841
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0042834
Disease:
Vital capacity 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11191847
rs11191847
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1570221
rs1570221
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		A 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs9419958
rs9419958
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0751676
Disease:
Basal Cell Cancer 		T 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs9419958
rs9419958
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0042133
Disease:
Uterine Fibroids 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs9419958
rs9419958
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0206710
Disease:
Basal Cell Neoplasm 		T 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs9419958
rs9419958
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0007117
Disease:
Basal cell carcinoma 		T 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs9419958
rs9419958
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C2242776
Disease:
Plexiform leiomyoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs111447985
rs111447985
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs12765878
rs12765878
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs11598018
rs11598018
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0085136
Disease:
Central Nervous System Neoplasms 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
dbSNP: rs11598018
rs11598018
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0017638
Disease:
Glioma 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443 2017
dbSNP: rs2995264
rs2995264
Entrez Id: 79991
Gene Symbol: STN1
STN1
CUI: C0025202
Disease:
melanoma 		G 0.700 GeneticVariation GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017