Sensitive

Systemic sclerosis

TNPO · rs10488631

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Systemic sclerosis compared to the general population. (GWAS Catalog, Nat Genet 2010, PMID:20383147)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Systemic sclerosis. (GWAS Catalog, Nat Genet 2010, PMID:20383147)

T/T Published research associates this genotype with typical/baseline likelihood of Systemic sclerosis — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2010, PMID:20383147)

Source: GWAS Catalog, Nat Genet 2010, PMID:20383147

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