RS782088056 TSPEAR
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Associated Conditions
Ectodermal dysplasia 14
hair/tooth type with or without hypohidrosis
Autosomal recessive nonsyndromic hearing loss 98
Inborn genetic diseases
Ectodermal dysplasia 14
hair/tooth type with or without hypohidrosis
Autosomal recessive nonsyndromic hearing loss 98
Inborn genetic diseases
Other Variants in TSPEAR