RS886041295 GRIN2B

Health Risk Chr 12:13615221
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
27
Intellectual disability
autosomal dominant 6
Complex neurodevelopmental disorder
Ovarian serous cystadenocarcinoma
Developmental and epileptic encephalopathy
27
Intellectual disability
autosomal dominant 6
Complex neurodevelopmental disorder
Ovarian serous cystadenocarcinoma
Other Variants in GRIN2B
rs1057519611 rs1060499526 rs387906636 rs1057519612 rs397514555 rs398122824 rs398122825 rs397514556 rs200608452 rs527236034
Ask Dr. Hemsworth about this variant