RS766500689 EDARADD

Health Risk Chr 1:236427427
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ectodermal dysplasia 11B
hypohidrotic/hair/tooth type
autosomal recessive
Ectodermal dysplasia 11B
hypohidrotic/hair/tooth type
autosomal recessive
Other Variants in EDARADD
rs74315309 rs121908116 rs879255629 rs879255553 rs759461234 rs1553271837 rs954823206 rs1005957166 rs1030214435 rs1657345576
Ask Dr. Hemsworth about this variant