Variant (rsID / SNP)

rs2834167

rs2834167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL10RB. Location: chromosome 21, position 34,640,788. Clinical significance in the table: Benign.

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Reference-table entries

IL10RBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:34640788
Cytoband: 21q22.11
HGVS: NM_000628.5(IL10RB):c.139A>G (p.Lys47Glu)
Allele change: Missense_K47E

Associated conditions / phenotypes

Hepatitis B virus, susceptibility to|Inflammatory bowel disease 25

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.