Sensitive
Coronary artery disease
ADAMTS7 · rs1994016
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What each result means
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coronary artery disease compared to the general population. (GWAS Catalog, Lancet 2011, PMID:21239051)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coronary artery disease. (GWAS Catalog, Lancet 2011, PMID:21239051)
T/T
Published research associates this genotype with typical/baseline likelihood of Coronary artery disease — no copies of the reported risk allele. (GWAS Catalog, Lancet 2011, PMID:21239051)
Source: GWAS Catalog, Lancet 2011, PMID:21239051
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