RS869312941 ARHGEF9

Health Risk Chr X:63665930
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy
8
Inborn genetic diseases
Developmental and epileptic encephalopathy
8
Other Variants in ARHGEF9
rs121918361 rs397514460 rs140777637 rs782497496 rs56375542 rs782577519 rs782248986 rs1057522347 rs782166488 rs1135401795
Ask Dr. Hemsworth about this variant