RS183480366 DCDC2
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Associated Conditions
Nephronophthisis 19
Isolated neonatal sclerosing cholangitis
Autosomal recessive nonsyndromic hearing loss 66
Inborn genetic diseases
Nephronophthisis 19
Isolated neonatal sclerosing cholangitis
Autosomal recessive nonsyndromic hearing loss 66
Inborn genetic diseases
Other Variants in DCDC2