RS672601378 GRIN2B

Health Risk Chr 12:13615149
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 6
Inborn genetic diseases
Developmental and epileptic encephalopathy
27
Intellectual disability
autosomal dominant 6
Inborn genetic diseases
Developmental and epileptic encephalopathy
27
Other Variants in GRIN2B
rs1057519611 rs1060499526 rs387906636 rs1057519612 rs397514555 rs398122824 rs398122825 rs397514556 rs200608452 rs527236034
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