TBX3, T-box transcription factor 3, 6926

N. diseases: 179; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768160499
rs768160499
Entrez Id: 6926;105370000
Gene Symbol: TBX3;LOC105370000
TBX3;LOC105370000
CUI: C1853238
Disease:
Conotruncal defect 		0.010 GeneticVariation BEFREE Our results indicate that the R608W and R616Q variants of TBX2 as well as the A192T and A562V variants of TBX3 contribute to CTD etiology; this was the first association of variants of TBX2 and TBX3 to CTDs based on a large population. 30223900 2018
dbSNP: rs8853
rs8853
Entrez Id: 6926
Gene Symbol: TBX3
TBX3
CUI: C1704272
Disease:
Benign Prostatic Hyperplasia 		C 0.700 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027 2018
dbSNP: rs8853
rs8853
Entrez Id: 6926
Gene Symbol: TBX3
TBX3
CUI: C0574785
Disease:
Lower Urinary Tract Symptoms 		C 0.700 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027 2018
dbSNP: rs1061651
rs1061651
Entrez Id: 6926
Gene Symbol: TBX3
TBX3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2242442
rs2242442
Entrez Id: 6926;105370000
Gene Symbol: TBX3;LOC105370000
TBX3;LOC105370000
CUI: C0948364
Disease:
Periprosthetic osteolysis 		A 0.700 GeneticVariation GWASCAT The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? 30794219 2019