Variant (rsID / SNP)
rs12979860
rs12979860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNL3, IFNL4. Location: chromosome 19, position 39,738,787. Clinical significance in the table: drug response.
Reference-table entries
IFNL3Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:39738787
- Cytoband
- 19q13.2
- HGVS
- NM_001276254.2(IFNL4):c.151-152G>A
- Allele change
- Silent
Associated conditions / phenotypes
peginterferon alfa-2a, peginterferon alfa-2b, ribavirin, and telaprevir response - Efficacy|peginterferon alfa-2a, peginterferon alfa-2b, and ribavirin response - Efficacy|boceprevir, peginterferon alfa-2a, peginterferon alfa-2b and ribavirin response - Efficacy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.