RS747806672 EDAR

Health Risk Chr 2:108897110
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
Ectodermal dysplasia 10A
hypohidrotic/hair/nail type
autosomal dominant
Ectodermal dysplasia 10B
hypohidrotic/hair/tooth type
autosomal recessive
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
Ectodermal dysplasia 10A
hypohidrotic/hair/nail type
autosomal dominant
Ectodermal dysplasia 10B
hypohidrotic/hair/tooth type
autosomal recessive
Other Variants in EDAR
rs1558814967 rs121908450 rs121908452 rs121908453 rs797044435 rs121908454 rs121908455 rs121908456 rs797044436 rs797044437
Ask Dr. Hemsworth about this variant