rs1057517513, SLC26A2

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Achondrogenesis, type IB (disorder)
CUI: C0265274
Disease: Achondrogenesis, type IB (disorder)
0.700 GeneticVariation CLINVAR Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. 26375458 2015
EPIPHYSEAL DYSPLASIA, MULTIPLE, 4
CUI: C1847593
Disease: EPIPHYSEAL DYSPLASIA, MULTIPLE, 4
0.700 GeneticVariation CLINVAR Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. 26375458 2015
Atelosteogenesis type 2
CUI: C1850554
Disease: Atelosteogenesis type 2
0.700 GeneticVariation CLINVAR Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. 26375458 2015
Diastrophic dysplasia
CUI: C0220726
Disease: Diastrophic dysplasia
0.700 GeneticVariation CLINVAR Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. 26375458 2015