Annotation Detail
Information
- Associated Genes
- IFNA13
- Associated Variants
-
IFNA13 MUTATION
IFNA13 MUTATION
FDFT1 c.879+739A>C ( ENST00000220584.9, ENST00000443614.6, ENST00000525900.5, ENST00000525954.5, ENST00000528643.5, ENST00000528812.5, ENST00000530337.6, ENST00000530664.5, ENST00000615631.4, ENST00000622850.3 )
FDFT1 c.879+739A>G ( ENST00000530664.5, ENST00000528643.5, ENST00000525954.5, ENST00000443614.6, ENST00000525900.5, ENST00000528812.5, ENST00000220584.9, ENST00000530337.6, ENST00000615631.4, ENST00000622850.3 )
FDFT1 c.879+739A>C ( ENST00000220584.9, ENST00000443614.6, ENST00000525900.5, ENST00000525954.5, ENST00000528643.5, ENST00000528812.5, ENST00000530337.6, ENST00000530664.5, ENST00000615631.4, ENST00000622850.3 )
FDFT1 c.879+739A>G ( ENST00000220584.9, ENST00000443614.6, ENST00000525900.5, ENST00000525954.5, ENST00000528643.5, ENST00000528812.5, ENST00000530337.6, ENST00000530664.5, ENST00000615631.4, ENST00000622850.3 ) - Associated Disease
- Hepatitis C, Chronic
- Source Database
- DisGeNET
- Description
- The SNPs rs738409478 and rs2645424 were determined by real-time PCR in 478 patients with CHC (m/f: 314/164; mean age: 44.9 ± 10.7; GT1: 387, GT4: 91) who completed treatment with peg-IFN-α-2a/ribavirin.All had a pretreatment liver biopsy.
- Pubmed
- 23870067
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.0306729315450743
- Year of publication
- 2013
Drugs