Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167433
rs1114167433
0.020 GeneticVariation BEFREE Increasing βB1-crystallin sensitivity to proteolysis caused by the congenital cataract-microcornea syndrome mutation S129R. 23159606

2013

dbSNP: rs1114167433
rs1114167433
0.020 GeneticVariation BEFREE A novel mutation in CRYBB1 associated with congenital cataract-microcornea syndrome: the p.Ser129Arg mutation destabilizes the βB1/βA3-crystallin heteromer but not the βB1-crystallin homomer. 21972112

2011

dbSNP: rs1114167432
rs1114167432
0.010 GeneticVariation BEFREE Congenital microcornea-cataract syndrome-causing mutation X253R increases βB1-crystallin hydrophobicity to promote aggregate formation. 27208166

2016

dbSNP: rs200090198
rs200090198
0.010 GeneticVariation BEFREE By sequencing the whole exome of three patients in a Chinese four-generation dominant CCMC family (Family A), three heterozygous missense mutation (c.115C>G, c.277G>A, and c.4393G>A) were identified in ATP-binding cassette protein A3 (ABCA3). 25406294

2014

dbSNP: rs201955122
rs201955122
0.010 GeneticVariation BEFREE By sequencing the whole exome of three patients in a Chinese four-generation dominant CCMC family (Family A), three heterozygous missense mutation (c.115C>G, c.277G>A, and c.4393G>A) were identified in ATP-binding cassette protein A3 (ABCA3). 25406294

2014

dbSNP: rs748819386
rs748819386
0.010 GeneticVariation BEFREE We further confirmed our finding by identifying another heterozygous missense mutation, c.2408C>T, in ABCA3 in an additional dominant CCMC family (Family B), which also cosegregated with the phenotype. 25406294

2014