RS199669988 ALPL

Health Risk Chr 1:21564097
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What This Variant Does
"rs199669988, also known as c.529G&gt
Associated Conditions
Infantile hypophosphatasia
Hypophosphatasia
Microcephaly
Adult hypophosphatasia
Inborn genetic diseases
Childhood hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Microcephaly
Adult hypophosphatasia
Inborn genetic diseases
Childhood hypophosphatasia
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
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