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Lack of Association of LRP8 SNP R952Q with Sporadic CAD and MI in the GeneBank Population (1,231 Cases) and 560 Controls
| MAF(%) |
P |
|||||
| SNP | Allelea | Cases | Controls | OR (95% CI) | Observedb | Adjustedc |
| R952Q | A | 39.1 | 37.8 | 1.06 (.82–1.09) | .439 | .253 |
Allele A at the nucleotide level corresponds to variant 952Q at the protein level.
Uncorrected P value.
P value obtained after adjustment for sex and age.
