RS764994176 ALPL

Health Risk Chr 1:21577647
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Associated Conditions
Infantile hypophosphatasia
Osteogenesis imperfecta
Inborn genetic diseases
Infantile hypophosphatasia
Osteogenesis imperfecta
Inborn genetic diseases
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant