RS121918008 ALPL

Health Risk Chr 1:21575868
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What This Variant Does
"rs121918008, also known as c.1133A&gt
Associated Conditions
Adult hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
Inborn genetic diseases
Adult hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
Inborn genetic diseases
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918009
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