Variant (rsID / SNP)

rs8099917

rs8099917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNL3. Location: chromosome 19, position 39,743,165. Clinical significance in the table: drug response.

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Reference-table entries

IFNL3Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:39743165
Cytoband: 19q13.2
HGVS: NC_000019.10:g.39252525T>G

Associated conditions / phenotypes

interferons, peginterferon alfa-2a, peginterferon alfa-2b, and ribavirin response - Efficacy|peginterferon alfa-2a, peginterferon alfa-2b, ribavirin, and telaprevir response - Efficacy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.