Sensitive
Celiac disease
IL12A · rs17810546
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What each result means
A/A
Published research associates this genotype with typical/baseline likelihood of Celiac disease — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2008, PMID:18311140)
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Celiac disease. (GWAS Catalog, Nat Genet 2008, PMID:18311140)
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Celiac disease compared to the general population. (GWAS Catalog, Nat Genet 2008, PMID:18311140)
Source: GWAS Catalog, Nat Genet 2008, PMID:18311140
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