RS375618091 KMT2B

Health Risk Chr 19:35720324
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Associated Conditions
Inborn genetic diseases
Intellectual developmental disorder
autosomal dominant 68
Dystonia 28
childhood-onset
Inborn genetic diseases
Intellectual developmental disorder
autosomal dominant 68
Dystonia 28
childhood-onset
Other Variants in KMT2B
rs1057519278 rs1057519279 rs1057519280 rs1057519281 rs1057519282 rs1057519283 rs1057519284 rs1057519285 rs1085307751 rs190929421
Ask Dr. Hemsworth about this variant