eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | sandhoff disease |
| Comorbidity | C0242379|lung cancer |
| Sentences | 3 |
| PubMedID- 20651612 | For xpd lys751gln genotype, significantly increased lung cancer risk was associated with two variant genotypes (cc versus aa: odds ratio [or] = 1.26, 95% confidence interval [ci] = 1.12-1.42, p = 0.473 for heterogeneity; c allele carriers versus aa: or = 1.18, 95% ci = 1.08-1.36, p = 0.732 for heterogeneity). |
| PubMedID- 22579698 | A significantly elevated lung cancer risk was associated with two variant genotypes (for tt vs cc: or=1.24, 95% ci=1.11-1.40; for ct and tt combined vs cc: or=1.19, 95% ci=1.12-1.27) in the overall population. |
| PubMedID- 24681604 | Concurrently, we observed cell type–specific effects for lung cancer with two variants located in cancer pleiotropic regions (tert and risk of lung adenocarcinoma and cdkn2bas1 with risk of lung scc), indicating distinct etiological processes for these two subtypes. |
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