RS886041847 SATB2

Health Risk Chr 2:199328799
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Chromosome 2q32-q33 deletion syndrome
Neurodevelopmental abnormality
Chromosome 2q32-q33 deletion syndrome
Neurodevelopmental abnormality
Other Variants in SATB2
rs137853127 rs797044874 rs863224917 rs2105928778 rs875989830 rs878853163 rs886039740 rs886041685 rs886041516 rs1057518614
Ask Dr. Hemsworth about this variant