RS2102345680 PBX1
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Associated Conditions
Inborn genetic diseases
PBX1-related disorder
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss
abnormal ears
or developmental delay
Inborn genetic diseases
PBX1-related disorder
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss
abnormal ears
or developmental delay
Other Variants in PBX1