RS387906635 GRIN1

Health Risk Chr 9:137162710
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Other Variants in GRIN1
rs1554770064 rs797044925 rs797045047 rs797045605 rs141473515 rs145176345 rs146086141 rs869312865 rs878853143 rs200225692
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