RS786204634 ALPL

Health Risk Chr 1:21570321
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What This Variant Does
"rs786204634, also known as c.809G&gt
Associated Conditions
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
Autosomal recessive ALPL-related disorders
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
Autosomal recessive ALPL-related disorders
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
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