RS878855327 ANKRD11

Health Risk Chr 16:89279749
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What This Variant Does
"CLNSIG=5
Associated Conditions
KBG syndrome
Inborn genetic diseases
Rare genetic intellectual disability
KBG syndrome
Epilepsy
KBG syndrome
Inborn genetic diseases
Rare genetic intellectual disability
KBG syndrome
Epilepsy
Other Variants in ANKRD11
rs863223319 rs863223320 rs863223321 rs797044900 rs797044890 rs797045027 rs863225257 rs201522384 rs869312713 rs1114167291
Ask Dr. Hemsworth about this variant