RS730882219 GEMIN4

Health Risk Chr 17:745591
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Microcephaly
Severe dystonia
Developmental cataract
Global developmental delay
Neurodevelopmental disorder with microcephaly
cataracts
and renal abnormalities
Microcephaly
Severe dystonia
Developmental cataract
Global developmental delay
Neurodevelopmental disorder with microcephaly
cataracts
and renal abnormalities
Other Variants in GEMIN4
rs199897496 rs201544259 rs188821606 rs143168627 rs878940028 rs200379895 rs180894698
Ask Dr. Hemsworth about this variant