RS121918011 ALPL

Health Risk Chr 1:21563219
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What This Variant Does
"rs121918011, also known as c.407G&gt
Associated Conditions
Childhood hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Osteogenesis imperfecta
Odontohypophosphatasia
ALPL-related autosomal recessive hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
Infantile hypophosphatasia
Hypophosphatasia
Adult hypophosphatasia
Osteogenesis imperfecta
Odontohypophosphatasia
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 1.86 2E-77 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant