Variant (rsID / SNP)
rs20541
rs20541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL13. Location: chromosome 5, position 131,995,964. Clinical significance in the table: risk factor.
Reference-table entries
IL13Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:131995964
- Cytoband
- 5q31.1
- HGVS
- NM_002188.3(IL13):c.431A>G (p.Gln144Arg)
- Allele change
- Missense_Q79R
Associated conditions / phenotypes
Inherited susceptibility to asthma|Allergic rhinitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.