Trait

SNPs associated with Inborn Disorder Of Amino Acid Metabolism

1 genetic variant across 1 genes have been associated with Inborn Disorder Of Amino Acid Metabolism in published research. Key genes include ZCCHC10.

Associated variants1 total

rsidGeneEffectEvidence
rs560463877ZCCHC10GWAS association (p=7.0e-12)Major Consortium Study

Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.

Inborn Disorder Of Amino Acid Metabolism — SNPs & genetic associations — Gene Wizard