RS104893920 SLC26A2

Health Risk Chr 5:149980866
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Achondrogenesis
type IB
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
Atelosteogenesis type II
Achondrogenesis
type IB
Diastrophic dysplasia
Multiple epiphyseal dysplasia type 4
Atelosteogenesis type II
Other Variants in SLC26A2
rs386833498 rs786200881 rs104893915 rs104893917 rs104893918 rs104893919 rs104893916 rs104893921 rs386833492 rs104893924
Ask Dr. Hemsworth about this variant