RUNX3, RUNX family transcription factor 3, 864

N. diseases: 281; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7536201
rs7536201
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0033860
Disease:
Psoriasis
C 0.800 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs7536201
rs7536201
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0033860
Disease:
Psoriasis
0.800 GeneticVariation GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs10794666
rs10794666
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs189131320
rs189131320
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified
G 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019
dbSNP: rs6672420
rs6672420
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7517302
rs7517302
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0004096
Disease:
Asthma
T 0.700 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
dbSNP: rs760805
rs760805
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C0013595
Disease:
Eczema
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9438876
rs9438876
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs742230
rs742230
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C1527304
Disease:
Allergic Reaction
0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
dbSNP: rs742230
rs742230
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C0004096
Disease:
Asthma
0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
dbSNP: rs1005734
rs1005734
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0002170
Disease:
Alopecia
A 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs188468174
rs188468174
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0002170
Disease:
Alopecia
T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs760805
rs760805
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C1527304
Disease:
Allergic Reaction
T 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs79598985
rs79598985
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0002170
Disease:
Alopecia
A 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs7536201
rs7536201
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0263361
Disease:
Psoriasis vulgaris
C 0.700 GeneticVariation GWASCAT Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. 26626624 2015
dbSNP: rs6672420
rs6672420
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE Evaluation of the differential expression between carcinoma and normal mucosa showed that SMAD3 rs12708491 and rs2414937, NFκB1 rs230510 and rs3821958, and RUNX3 rs6672420 were associated with several miRNAs for colorectal carcinoma. 28061442 2017
dbSNP: rs6672420
rs6672420
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE The RUNX3 rs2236852 AA genotype and A allele showed association with CRC (OR = 0.39, 95%CI = 0.21-0.73, P < 0.01; OR = 0.65, 95%CI = 0.49-0.87, P < 0.01, respectively), while the rs6672420, rs11249206, and rs760805 polymorphisms did not show significant association with CRC. 26634516 2015
dbSNP: rs6672420
rs6672420
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0036421
Disease:
Systemic Scleroderma
0.010 GeneticVariation BEFREE A higher methylation status of the <i>RUNX3</i> gene, which is associated with polymorphism rs6672420, correlates with lower <i>RUNX3</i> expression and SSc susceptibility. 31126957 2019
dbSNP: rs760805
rs760805
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C0004045
Disease:
Asphyxia Neonatorum
0.010 GeneticVariation BEFREE Compared with rs760805 TT homozygote carriers, patients carrying AA homozygote exhibited significantly reduced 24 hours urinary protein levels, lower serum creatinine concentrations and a decreased incidence of neonatal asphyxia (P <.05).The present study suggested a genetic association between RUNX3 gene polymorphisms and SPE. 30896667 2019
dbSNP: rs11249206
rs11249206
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The RUNX3 rs2236852 AA genotype and A allele showed association with CRC (OR = 0.39, 95%CI = 0.21-0.73, P < 0.01; OR = 0.65, 95%CI = 0.49-0.87, P < 0.01, respectively), while the rs6672420, rs11249206, and rs760805 polymorphisms did not show significant association with CRC. 26634516 2015
dbSNP: rs2236852
rs2236852
Entrez Id: 864
Gene Symbol: RUNX3
RUNX3
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The RUNX3 rs2236852 AA genotype and A allele showed association with C</span>RC (OR = 0.39, 95%CI = 0.21-0.73, P < 0.01; OR = 0.65, 95%CI = 0.49-0.87, P < 0.01, respectively), while the rs6672420, rs11249206, and rs760805 polymorphisms did not show significant association with CRC. 26634516 2015
dbSNP: rs760805
rs760805
Entrez Id: 864;107984932
Gene Symbol: RUNX3;LOC107984932
RUNX3;LOC107984932
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The RUNX3 rs2236852 AA genotype and A allele showed association with CRC (OR = 0.39, 95%CI = 0.21-0.73, P < 0.01; OR = 0.65, 95%CI = 0.49-0.87, P < 0.01, respectively), while the rs6672420, rs11249206, and rs760805 polymorphisms did not show significant association with CRC. 26634516 2015
dbSNP: rs1395621
rs1395621
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0038013
Disease:
Ankylosing spondylitis
0.010 GeneticVariation BEFREE The rs7379457 SNP in PPARGC1B, the rs1395621 and rs9438876 SNPs in RUNX3, and the rs8070463 SNP in TBKBP1 are related to the severity of AS in Chinese Han population. 23637848 2013
dbSNP: rs906296
rs906296
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE After adjustment for multiple comparisons, two SNPs were significantly associated with breast cancer risk: RUNX3 (rs906296 ORCG/GG = 1.15 95 % CI 1.04-1.26) and TGF-β1 (rs4803455 ORCA/AA = 0.89 95 % CI 0.81-0.98). 24036662 2013
dbSNP: rs906296
rs906296
Entrez Id: 864;105376878
Gene Symbol: RUNX3;LOC105376878
RUNX3;LOC105376878
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE After adjustment for multiple comparisons, two SNPs were significantly associated with breast cancer risk: RUNX3 (rs906296 ORCG/GG = 1.15 95 % CI 1.04-1.26) and TGF-β1 (rs4803455 ORCA/AA = 0.89 95 % CI 0.81-0.98). 24036662 2013