Annotation Detail
Information
- Associated Genes
- PTPN22
- Associated Variants
-
PTPN22 MUTATION
PTPN22 MUTATION - Associated Disease
- Secondary antiphospholipid syndrome
- Source Database
- DisGeNET
- Description
- Significant association of the PTPN22 T1858 allele (CT + TT vs.CC) and secondary antiphospholipid syndrome was observed (p = 0.049).
- Pubmed
- 24985973
- Section of the abstract supporting the evidence
- ALL_TEXT_3/3
- Number of the section of the abstract supporting the evidence
- 3
- Number of the sentence supporting the evidence
- 7
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs