Variant (rsID / SNP)

rs9005

rs9005 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL1RN. Location: chromosome 2, position 113,891,412. Clinical significance in the table: Benign.

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Reference-table entries

IL1RNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:113891412
Cytoband: 2q14.1
HGVS: NM_173842.3(IL1RN):c.*964G>A
Allele change: Silent

Associated conditions / phenotypes

Sterile multifocal osteomyelitis with periostitis and pustulosis

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.