RS369318758 SLC26A2
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Associated Conditions
Achondrogenesis
type IB
Multiple epiphyseal dysplasia type 4
Diastrophic dysplasia
Atelosteogenesis type II
Inborn genetic diseases
Achondrogenesis
type IB
Multiple epiphyseal dysplasia type 4
Diastrophic dysplasia
Atelosteogenesis type II
Inborn genetic diseases
Other Variants in SLC26A2