RS121918009 ALPL

Health Risk Chr 1:21575736
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What This Variant Does
"rs121918009, also known as c.1001G&gt
Associated Conditions
Infantile hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Osteogenesis imperfecta
ALPL-related disorder
Infantile hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Osteogenesis imperfecta
ALPL-related disorder
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
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