RS1060499602 ASXL3

Health Risk Chr 18:33738875
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
Intellectual disability
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
Intellectual disability
Other Variants in ASXL3
rs587777061 rs587777062 rs1555742148 rs797045317 rs151027205 rs371181408 rs189786599 rs201776257 rs869312696 rs886039650
Ask Dr. Hemsworth about this variant