SLC26A2, solute carrier family 26 member 2, 1836

N. diseases: 198; N. variants: 78
Disease: EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517511
rs1057517511
Entrez Id: 1836
Gene Symbol: SLC26A2
SLC26A2
CUI: C1847593
Disease:
EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 		AGTTAT 0.700 GeneticVariation CLINVAR