SMAD3, SMAD family member 3, 4088

N. diseases: 470; N. variants: 95
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12913547
rs12913547
Entrez Id: 4088
Gene Symbol: SMAD3
SMAD3
CUI: C0524957
Disease:
Corneal Topography
T 0.800 GeneticVariation GWASCAT Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. 23291589 2013
dbSNP: rs12913547
rs12913547
Entrez Id: 4088
Gene Symbol: SMAD3
SMAD3
CUI: C0524957
Disease:
Corneal Topography
T 0.800 GeneticVariation GWASDB Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. 23291589 2013