RS2102345684 PBX1

Health Risk Chr 1:164812020
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Associated Conditions
Inborn genetic diseases
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss
abnormal ears
or developmental delay
Inborn genetic diseases
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss
abnormal ears
or developmental delay
Other Variants in PBX1
rs1553247028 rs1553248081 rs1553248075 rs1553247020 rs1553248110 rs1553248112 rs1553249136 rs1553249146 rs1558020021 rs866426234
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