RS371243939 ALPL

Health Risk Chr 1:21575906
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs371243939, also known as c.1171C&gt
Associated Conditions
Infantile hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
Inborn genetic diseases
ALPL-related disorder
Infantile hypophosphatasia
Adult hypophosphatasia
Childhood hypophosphatasia
Hypophosphatasia
Osteogenesis imperfecta
Inborn genetic diseases
ALPL-related disorder
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 1.88 3E-108 PubMed
Serum phosphate levels — OR: 0.83 7E-16 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant