RS786204675 SLC26A2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Multiple epiphyseal dysplasia type 4
Sulfate transporter-related osteochondrodysplasia
Diastrophic dysplasia
Achondrogenesis
type IB
Atelosteogenesis type II
Multiple epiphyseal dysplasia type 4
Sulfate transporter-related osteochondrodysplasia
Diastrophic dysplasia
Achondrogenesis
type IB
Atelosteogenesis type II
Other Variants in SLC26A2