Variant (rsID / SNP)

rs11209026

rs11209026 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL23R. Location: chromosome 1, position 67,705,958. Clinical significance in the table: Benign.

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Reference-table entries

IL23RBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:67705958
Cytoband: 1p31.3
HGVS: NM_144701.3(IL23R):c.1142G>A (p.Arg381Gln)
Allele change: Missense_R381Q

Associated conditions / phenotypes

Inflammatory bowel disease 17, protection against|Psoriasis, protection against

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.