RS75097996 SLC26A2
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Associated Conditions
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
Atelosteogenesis type II
Diastrophic dysplasia
Inborn genetic diseases
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
Atelosteogenesis type II
Diastrophic dysplasia
Inborn genetic diseases
Other Variants in SLC26A2