Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		C 0.800 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577

2009
dbSNP: rs273909
rs273909
SLC22A4 ; MIR3936HG
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013
dbSNP: rs10058074
rs10058074
MIR3936HG
CUI: C0489786
Disease: Height
Height 		A 0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607

2013
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		C 0.700 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577

2009
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		C 0.700 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577

2009
dbSNP: rs270607
rs270607
SLC22A4 ; MIR3936HG
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs270607
rs270607
SLC22A4 ; MIR3936HG
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs270607
rs270607
SLC22A4 ; MIR3936HG
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		0.700 GeneticVariation GWASDB Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). 20978265

2011
dbSNP: rs272888
rs272888
SLC22A4 ; MIR3936HG
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs272889
rs272889
SLC22A4 ; MIR3936HG
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		A 0.700 GeneticVariation GWASDB Human metabolic individuality in biomedical and pharmaceutical research. 21886157

2011
dbSNP: rs272889
rs272889
SLC22A4 ; MIR3936HG
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		A 0.700 GeneticVariation GWASDB Human metabolic individuality in biomedical and pharmaceutical research. 21886157

2011
dbSNP: rs274546
rs274546
MIR3936HG
CUI: C0489786
Disease: Height
Height 		0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960

2010