RS886041505 CACNA1G

Health Risk Chr 17:50592063
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia 42
early-onset
severe
with neurodevelopmental deficits
Neurodevelopmental abnormality
Inborn genetic diseases
Spinocerebellar ataxia 42
early-onset
severe
with neurodevelopmental deficits
Neurodevelopmental abnormality
Other Variants in CACNA1G
rs730882202 rs543673731 rs755221106 rs886039324 rs200141555 rs763813233 rs757227515 rs947131228 rs757138454 rs771214256
Ask Dr. Hemsworth about this variant