RS386833492 SLC26A2

Health Risk Chr 5:149960981
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What This Variant Does
"A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in ...
Associated Conditions
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
Atelosteogenesis type II
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
3MC syndrome 2
SLC26A2-related disorder
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
Atelosteogenesis type II
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
3MC syndrome 2
Other Variants in SLC26A2
rs386833498 rs786200881 rs104893915 rs104893917 rs104893918 rs104893919 rs104893920 rs104893916 rs104893921 rs104893924
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