Annotation Detail
Information
- Associated Genes
- XRCC1
- Associated Variants
-
XRCC1 MUTATION
XRCC1 MUTATION - Associated Disease
- Pseudoaphakia
- Source Database
- DisGeNET
- Description
- Various combinations of the keywords and MeSH terms were used to screen for potentially relevant studies, specifically genetic polymorphisms or SNPs or variation or single nucleotide polymorphism or polymorphism or mutation or variant; X-ray repair cross complementing protein 1 or Xeroderma Pigmentosum Group D Protein or X-ray repair cross complementing protein 1 or Xeroderma Pigmentosum Group D Protein or XPD or Xeroderma Pigmentosum Complementation Group D Protein or ERCC2 or XRCC1 or XRCC1 DNA repair protein; and Cataract or Membranous Cataract or Pseudoaphakia. Meta-analyses were conducted using Stata 12.0 software.
- Pubmed
- 25873778
- Section of the abstract supporting the evidence
- METHODS
- Number of the section of the abstract supporting the evidence
- 2
- Number of the sentence supporting the evidence
- 3
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs