Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909209
rs121909209
TGFBI
0.040 GeneticVariation BEFREE In this Chinese family an R555Q mutation of the TGFBI gene was associated with RBCD. 22906289

2012
dbSNP: rs121909209
rs121909209
TGFBI
0.040 GeneticVariation BEFREE Two patients from one pedigree (a 29-year-old woman and 58-year-old man) with Thiel-Behnke corneal dystrophy (Arg555Gln [R555Q] heterozygous missense mutation of human transforming growth factor beta-induced [TGFBI] gene) and 3 patients from one pedigree (a 70-year-old woman, 58-year-old man, and 14-year old man) with Reis-Bücklers corneal dystrophy (Arg124Leu [R124L] heterozygous missense mutation of the TGFBI gene) were examined. 17198850

2007
dbSNP: rs121909209
rs121909209
TGFBI
0.040 GeneticVariation BEFREE A R555Q mutation was detected in the patients with RBCD. 11095060

2000
dbSNP: rs121909209
rs121909209
TGFBI
0.040 GeneticVariation BEFREE The variant of RBCD characterized by honeycomb-shaped opacities is caused by an Arg555Gln kerato-epithelin mutation. 9780098

1998