RS121918002 ALPL

Health Risk Chr 1:21573683
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What This Variant Does
"rs121918002, also known as c.881A&gt
Associated Conditions
Infantile hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
ALPL-related disorder
Inborn genetic diseases
Infantile hypophosphatasia
Childhood hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
ALPL-related disorder
Inborn genetic diseases
GWAS Studies (4)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 2.41 8E-296 PubMed
Serum alkaline phosphatase levels C OR: 2.33 3E-154 PubMed
Serum phosphate levels — OR: 0.98 5E-38 PubMed
Serum phosphate levels C OR: 0.93 3E-23 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008 rs121918009
Ask Dr. Hemsworth about this variant