RS869025220 DVL1

Health Risk Chr 1:1338093
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant Robinow syndrome 2
Autosomal dominant Robinow syndrome 2
Other Variants in DVL1
rs797044837 rs797044840 rs797044833 rs797044839 rs797044838 rs797044835 rs797044834 rs797044836 rs1057518627 rs372681220
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