Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss

Renal 37 variants 1 gene

Upload your DNA to see your personal risk score for Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss.

Associated Genes (1)
Associated Variants (37)
RSID Gene Risk Allele Odds Ratio Evidence
RS2526855476 PBX1 strong
RS2101688490 PBX1 strong
RS2101678386 PBX1 strong
RS2102345684 PBX1 strong
RS2102319647 PBX1 strong
RS2102319548 PBX1 strong
RS2102302158 PBX1 strong
RS1218945005 PBX1 strong
RS1423937629 PBX1 strong
RS2526809677 PBX1 strong
RS2102302170 PBX1 strong
RS2102345680 PBX1 strong
RS1259895025 PBX1 strong
RS2526809998 PBX1 strong
RS2526810620 PBX1 strong
RS2526855331 PBX1 strong
RS2525299549 PBX1 strong
RS2526810325 PBX1 strong
RS2525299908 PBX1 strong
RS1571217834 PBX1 strong
RS1553248081 PBX1 strong
RS1553248075 PBX1 strong
RS1553247020 PBX1 strong
RS1553248110 PBX1 strong
RS1553248112 PBX1 strong
RS1553249136 PBX1 strong
RS1553249146 PBX1 strong
RS1558020021 PBX1 strong
RS1553247028 PBX1 strong
RS1571431145 PBX1 strong
RS1571431063 PBX1 strong
RS1571445295 PBX1 strong
RS773334722 PBX1 strong
RS1669421181 PBX1 strong
RS1668978337 PBX1 strong
RS2102336635 PBX1 strong
RS544057798 PBX1 strong
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