RS267607016 ROR2

Health Risk Chr 9:91726603
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What This Variant Does
"CLNSIG=5
Associated Conditions
Robinow syndrome
autosomal recessive
with brachy-syn-polydactyly
Autosomal recessive Robinow syndrome
Brachydactyly type B1
Robinow syndrome
autosomal recessive
with brachy-syn-polydactyly
Autosomal recessive Robinow syndrome
Brachydactyly type B1
Other Variants in ROR2
rs121909082 rs104894122 rs863223289 rs121909083 rs121909084 rs121909085 rs121909086 rs863223290 rs104894121 rs863223291
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