In the knowledge base ยท computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Aflatoxin-Related Hepatocellular Carcinoma modifier
Spinocerebellar Ataxia, Autosomal Recessive 26 causative germline loss of function
mechanism: Biallelic XRCC1 Variants; Reduced XRCC1 and DNA Ligase III Alpha Protein

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.