RS121918010 ALPL

Health Risk Chr 1:21573781
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What This Variant Does
"rs121918010, also known as c.979T&gt
Associated Conditions
Infantile hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
Infantile hypophosphatasia
Adult hypophosphatasia
Hypophosphatasia
Childhood hypophosphatasia
ALPL-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Serum alkaline phosphatase levels C OR: 1.04 6E-186 PubMed
Other Variants in ALPL
rs121918000 rs121918001 rs121918002 rs121918003 rs121918004 rs121918005 rs121918006 rs121918017 rs121918007 rs121918008
Ask Dr. Hemsworth about this variant