Variant (rsID / SNP)

rs228942

rs228942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL2RB. Location: chromosome 22, position 37,524,619. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IL2RBNot classified

Variant type: missense_variant
Chromosome / position: 22:37524619
HGVS: NM_000878.5,c.1173C>A,p.Asp391Glu
Allele change: Missense_D391E

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.