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ALPL rs1057516230: what the research says

rs1057516230
Trait
Moderate evidenceGene: ALPL

This variant in the ALPL gene is identified as a common clinical finding in genomic databases.

Common

Our full long-form research profile for rs1057516230 — genotype interpretations, evidence review, and FAQ — is being written and will appear on this page soon.
dbSNP ClinVar GWAS Catalog Google Scholar

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Related variants in ALPL

rs34810399
ALPL
Carrier Status
Moderate

This variant is associated with hypophosphatasia, a rare metabolic bone disorder, and identifies carriers of the pathogenic allele.