RS146787541 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
Inborn genetic diseases
Other Variants in DCDC2