RS386833497 SLC26A2

Health Risk Chr 5:149981243
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
SLC26A2-related disorder
Achondrogenesis
type IB
Atelosteogenesis type II
Osteochondrodysplasia
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
SLC26A2-related disorder
Achondrogenesis
type IB
Atelosteogenesis type II
Osteochondrodysplasia
Other Variants in SLC26A2
rs386833498 rs786200881 rs104893915 rs104893917 rs104893918 rs104893919 rs104893920 rs104893916 rs104893921 rs386833492
Ask Dr. Hemsworth about this variant