Variant (rsID / SNP)

rs1805015

rs1805015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL4R. Location: chromosome 16, position 27,374,180. Clinical significance in the table: protective.

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Reference-table entries

IL4RProtective

Clinical significance (as recorded): protective
Variant type: single nucleotide variant
Chromosome / position: 16:27374180
Cytoband: 16p12.1
HGVS: NM_000418.4(IL4R):c.1507T>C (p.Ser503Pro)
Allele change: Missense_S343P

Associated conditions / phenotypes

Atopy, resistance to

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.