RS781510673 DCDC2

Health Risk Chr 6:24302044
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Associated Conditions
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Nephronophthisis 19
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 66
Isolated neonatal sclerosing cholangitis
Nephronophthisis 19
Inborn genetic diseases
Other Variants in DCDC2
rs794729665 rs730880299 rs757704417 rs760040426 rs1042640142 rs1050411259 rs904944428 rs904520404 rs1554144869 rs41271773
Ask Dr. Hemsworth about this variant