RS869025217 DVL3

Health Risk Chr 3:184170318
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant Robinow syndrome 1
Autosomal dominant Robinow syndrome 3
Autosomal dominant Robinow syndrome 2
Autosomal dominant Robinow syndrome 3
Autosomal dominant Robinow syndrome 1
Autosomal dominant Robinow syndrome 3
Autosomal dominant Robinow syndrome 2
Autosomal dominant Robinow syndrome 3
Other Variants in DVL3
rs869025215 rs869025216 rs869025218 rs869025219 rs1553811652 rs753876000 rs1577052471 rs201329929 rs1577052755 rs1577052785
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