Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.800 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		C 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		C 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs12473028
rs12473028
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2048240
rs2048240
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs4666070
rs4666070
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7562
rs7562
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C1527304
Disease:
Allergic Reaction 		T 0.700 GeneticVariation GWASCAT Eleven loci with new reproducible genetic associations with allergic disease risk. 29679657 2019
dbSNP: rs7562
rs7562
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7606480
rs7606480
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11677002
rs11677002
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C2607914
Disease:
Allergic rhinitis (disorder) 		T 0.700 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184 2018
dbSNP: rs11680860
rs11680860
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0018498
Disease:
Hair Color 		A 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018
dbSNP: rs7562
rs7562
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. 28135244 2017
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0009324
Disease:
Ulcerative Colitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0038013
Disease:
Ankylosing spondylitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0008313
Disease:
Cholangitis, Sclerosing 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2279990
rs2279990
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs925255
rs925255
Entrez Id: 2355;403150
Gene Symbol: FOSL2;FLJ31356
FOSL2;FLJ31356
CUI: C0010346
Disease:
Crohn Disease 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015