RS760040426 DCDC2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Nephronophthisis 19
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Nephronophthisis 19
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Other Variants in DCDC2