RS1060505041 NACC1

Health Risk Chr 19:13136099
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What This Variant Does
"aka c.892C&gt
Associated Conditions
Neurodevelopmental disorder with epilepsy
cataracts
feeding difficulties
and delayed brain myelination
Inborn genetic diseases
NACC1-related disorder
Neurodevelopmental disorder with epilepsy
cataracts
feeding difficulties
and delayed brain myelination
Inborn genetic diseases
NACC1-related disorder
Other Variants in NACC1
rs2145625752 rs2019693030 rs2019737049 rs2145624427 rs748364235 rs2145623385 rs2019706242 rs2145623884 rs1330937800 rs767833951
Ask Dr. Hemsworth about this variant