RS774592932 GRIN2B

Health Risk Chr 12:13615213
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 6
Complex neurodevelopmental disorder
Developmental and epileptic encephalopathy
27
Complex neurodevelopmental disorder
Intellectual disability
autosomal dominant 6
Complex neurodevelopmental disorder
Developmental and epileptic encephalopathy
27
Complex neurodevelopmental disorder
Other Variants in GRIN2B
rs1057519611 rs1060499526 rs387906636 rs1057519612 rs397514555 rs398122824 rs398122825 rs397514556 rs200608452 rs527236034
Ask Dr. Hemsworth about this variant