RS863223291 ROR2

Health Risk Chr 9:91724551
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive Robinow syndrome
Autosomal recessive Robinow syndrome
Other Variants in ROR2
rs121909082 rs104894122 rs863223289 rs121909083 rs121909084 rs121909085 rs121909086 rs863223290 rs104894121 rs121909087
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