RS141060456 DCDC2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
DCDC2-related disorder
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
DCDC2-related disorder
Other Variants in DCDC2