Variant (rsID / SNP)

rs163897

rs163897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL5RA. Location: chromosome 3, position 3,115,478. The table records no clinical significance for this variant.

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Reference-table entries

IL5RANot classified

Variant type: intron_variant
Chromosome / position: 3:3115478
HGVS: NM_000564.5,c.1176+988A>G
Allele change: Silent

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.