RS763159520 ALPL

Health Risk Chr 1:21564118
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What This Variant Does
"rs763159520, also known as c.550C&gt
Associated Conditions
Inborn genetic diseases
Infantile hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
Adult hypophosphatasia
Odontohypophosphatasia
Inborn genetic diseases
Infantile hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
Adult hypophosphatasia
Odontohypophosphatasia
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
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