RS150800017 KMT2A

Health Risk Chr 11:118489816
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
KMT2A-related disorder
Inborn genetic diseases
KMT2A-related disorder
Other Variants in KMT2A
rs398122878 rs398122879 rs398122880 rs387907275 rs398122881 rs587783678 rs587783676 rs587783679 rs587783680 rs727503777
Ask Dr. Hemsworth about this variant