rs1800896
NC_000001.11:g.206773552T>C
- Leprosy, susceptibility to, 1Uncertain significance · inherited
gnomAD allele frequency 4.04e-1
rs1800896 is a genetic variant located in the IL10 gene. dbsnp · gene
In gnomAD, rs1800896 has an overall allele frequency of 40.4%. gnomad · frequency
In ClinVar, rs1800896 is classified as Uncertain significance (risk factor) for Leprosy, susceptibility to, 1 (0 review stars, inherited; last evaluated 2022-06-10). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 5a9e4504081bffbe · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0
Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.