RS398122823 GRIN2B

Health Risk Chr 12:13866109
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 6
Developmental and epileptic encephalopathy
27
Inborn genetic diseases
Intellectual disability
autosomal dominant 6
Developmental and epileptic encephalopathy
27
Inborn genetic diseases
Other Variants in GRIN2B
rs1057519611 rs1060499526 rs387906636 rs1057519612 rs397514555 rs398122824 rs398122825 rs397514556 rs200608452 rs527236034
Ask Dr. Hemsworth about this variant