RS148405563 ALPL

Health Risk Chr 1:21570330
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What This Variant Does
"rs148405563, also known as c.818C&gt
Associated Conditions
Hypophosphatasia
Inborn genetic diseases
ALPL-related disorder
Hypophosphatasia
Inborn genetic diseases
ALPL-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels — OR: 0.83 5E-81 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant