RS202213533 ROR2

Health Risk Chr 9:91723796
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Associated Conditions
Brachydactyly type B1
Autosomal recessive Robinow syndrome
Inborn genetic diseases
Brachydactyly type B1
Autosomal recessive Robinow syndrome
Inborn genetic diseases
Other Variants in ROR2
rs121909082 rs104894122 rs863223289 rs121909083 rs121909084 rs121909085 rs121909086 rs863223290 rs104894121 rs863223291
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