rs1553200431, COL11A1

N. diseases: 8
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myopia
CUI: C0027092
Disease: Myopia
0.700 GeneticVariation CLINVAR
Telecanthus
CUI: C0423113
Disease: Telecanthus
0.700 GeneticVariation CLINVAR
Dysmorphic facies
CUI: C0424503
Disease: Dysmorphic facies
0.700 GeneticVariation CLINVAR
Hypoplasia of the maxilla
CUI: C0240310
Disease: Hypoplasia of the maxilla
0.700 GeneticVariation CLINVAR
Congenital keratoglobus
CUI: C0344530
Disease: Congenital keratoglobus
0.700 GeneticVariation CLINVAR
Orbital separation excessive
CUI: C0020534
Disease: Orbital separation excessive
0.700 GeneticVariation CLINVAR
Short nose
CUI: C1854114
Disease: Short nose
0.700 GeneticVariation CLINVAR
Uranostaphyloschisis
CUI: C2981150
Disease: Uranostaphyloschisis
0.700 GeneticVariation CLINVAR