rs1423415130, XYLT2

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cataract
CUI: C0086543
Disease: Cataract
0.700 GeneticVariation CLINVAR
Shield chest
CUI: C1834124
Disease: Shield chest
0.700 GeneticVariation CLINVAR
Spondylo-ocular syndrome
CUI: C4225412
Disease: Spondylo-ocular syndrome
0.700 GeneticVariation CLINVAR
Retinal Detachment
CUI: C0035305
Disease: Retinal Detachment
0.700 GeneticVariation CLINVAR
Compression fracture of vertebral column
CUI: C0262431
Disease: Compression fracture of vertebral column
0.700 GeneticVariation CLINVAR
Osteopenia
CUI: C0029453
Disease: Osteopenia
0.700 GeneticVariation CLINVAR