RS121918007 ALPL

Health Risk Chr 1:21564139
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What This Variant Does
"rs121918007, also known as c.571G&gt
Associated Conditions
Infantile hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Odontohypophosphatasia
Inborn genetic diseases
Osteogenesis imperfecta
See cases
ALPL-related disorder
Adult hypophosphatasia
Infantile hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Odontohypophosphatasia
GWAS Studies (4)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 1.49 5E-398 PubMed
Serum alkaline phosphatase levels A OR: 1.52 2E-243 PubMed
Serum alkaline phosphatase levels A OR: 1.27 3E-51 PubMed
Choline phosphate levels A OR: 0.53 4E-15 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918008 rs121918009
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