RS758508750 DVL1

Health Risk Chr 1:1341688
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Associated Conditions
Autosomal dominant Robinow syndrome 2
Inborn genetic diseases
Autosomal dominant Robinow syndrome 2
Inborn genetic diseases
Other Variants in DVL1
rs797044837 rs797044840 rs797044833 rs797044839 rs797044838 rs797044835 rs797044834 rs797044836 rs869025220 rs1057518627
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