RS886041091 NTRK2

Health Risk Chr 9:84751990
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Developmental and epileptic encephalopathy
58
Inborn genetic diseases
Developmental and epileptic encephalopathy
58
Inborn genetic diseases
Other Variants in NTRK2
rs121434633 rs1085308029 rs201773066 rs1554774973 rs78936193 rs142393662 rs772111782 rs2131695386 rs145968424 rs1373336521
Ask Dr. Hemsworth about this variant