RS374692915 SLC26A2
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Associated Conditions
Atelosteogenesis type II
Sulfate transporter-related osteochondrodysplasia
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Diastrophic dysplasia
Inborn genetic diseases
Atelosteogenesis type II
Sulfate transporter-related osteochondrodysplasia
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Diastrophic dysplasia
Inborn genetic diseases
Other Variants in SLC26A2