RS797044874 SATB2

Health Risk Chr 2:199349027
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Chromosome 2q32-q33 deletion syndrome
SATB2 associated disorder
SATB2-related disorder
Inborn genetic diseases
Chromosome 2q32-q33 deletion syndrome
SATB2 associated disorder
SATB2-related disorder
Other Variants in SATB2
rs137853127 rs863224917 rs2105928778 rs875989830 rs878853163 rs886039740 rs886041847 rs886041685 rs886041516 rs1057518614
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