RS199665722 ALPL

Health Risk Chr 1:21568123
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What This Variant Does
"rs199665722, also known as c.668G&gt
Associated Conditions
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 3.1 3E-22 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant