Variant (rsID / SNP)

rs1043261

rs1043261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17RB. Location: chromosome 3, position 53,899,276. The table records no clinical significance for this variant.

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Reference-table entries

IL17RBNot classified

Variant type: stop_gained
Chromosome / position: 3:53899276
HGVS: NM_018725.4,c.1450C>T,p.Gln484*
Allele change: Nonsense_Q484X

Associated conditions / phenotypes

Interleukin-7 Receptor Alpha Deficiency|Type 1 Diabetes Mellitus

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.