RS139051143 SLC26A2

Health Risk Chr 5:149980673 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Diastrophic dysplasia
Atelosteogenesis type II
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
Connective tissue disorder
Diastrophic dysplasia
Atelosteogenesis type II
Multiple epiphyseal dysplasia type 4
Achondrogenesis
type IB
Sulfate transporter-related osteochondrodysplasia
Connective tissue disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in SLC26A2
rs386833498 rs786200881 rs104893915 rs104893917 rs104893918 rs104893919 rs104893920 rs104893916 rs104893921 rs386833492
Ask Dr. Hemsworth about this variant