Variant (rsID / SNP)

rs1800872

rs1800872 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL10. Location: chromosome 1, position 206,946,407. Clinical significance in the table: Benign.

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Reference-table entries

IL10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:206946407
Cytoband: 1q32.1
HGVS: NM_153758.5(IL19):c.-149+1984T>G

Associated conditions / phenotypes

Susceptibility to HIV infection|Graft-versus-host disease, resistance to|Inflammatory bowel disease

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.