| Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
Monocyte count result
|
0.700 | GeneticVariation | GWASCAT | Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. | 29403010 | 2018 | |||||
Monocyte count procedure
|
0.700 | GeneticVariation | GWASCAT | Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. | 29403010 | 2018 | |||||
Monocyte count procedure
|
0.700 | GeneticVariation | GWASCAT | Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. | 28158719 | 2017 | |||||
Monocyte count result
|
0.700 | GeneticVariation | GWASCAT | Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. | 28158719 | 2017 | |||||
Monocyte count result
|
0.700 | GeneticVariation | GWASCAT | Genetic variation associated with circulating monocyte count in the eMERGE Network. | 23314186 | 2013 | |||||
Monocyte count procedure
|
0.700 | GeneticVariation | GWASCAT | Genetic variation associated with circulating monocyte count in the eMERGE Network. | 23314186 | 2013 | |||||
Polysomnography
|
0.700 | GeneticVariation | GWASDB | Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. | 23251661 | 2012 | |||||
Secondary malignant neoplasm of lymph node
|
0.020 | GeneticVariation | BEFREE | Our previous research clarified two functional nonsynonymous single nucleotide polymorphisms (SNPs): rs12075 in DARC and rs2228468 in CCBP2 were significantly correlated with lymph node metastasis. | 30358125 | 2018 | |||||
Secondary malignant neoplasm of lymph node
|
0.020 | GeneticVariation | BEFREE | Two non-synonymous SNPs, rs12075 (G42D) in DARC and rs2228468 (S373Y) in CCBP2, were observed to be associated with LNM in univariate analysis and remained significant after adjustment for conventional clinical risk factors, with odds ratios (ORs) of 0.54 (95% confidence interval [CI], 0.37 to 0.79) and 0.78 (95% CI, 0.62 to 0.98), respectively. | 24260134 | 2013 | |||||
Secondary malignant neoplasm of lymph node
|
0.020 | GeneticVariation | BEFREE | Two non-synonymous SNPs, rs12075 (G42D) in DARC and rs2228468 (S373Y) in CCBP2, were observed to be associated with LNM in univariate analysis and remained significant after adjustment for conventional clinical risk factors, with odds ratios (ORs) of 0.54 (95% confidence interval [CI], 0.37 to 0.79) and 0.78 (95% CI, 0.62 to 0.98), respectively. | 24260134 | 2013 | |||||
Breast Carcinoma
|
0.010 | GeneticVariation | BEFREE | In the present study, rs12075 in DARC and rs2228468 in CCBP2 were genotyped in 806 patients with primary breast cancer. | 30358125 | 2018 | |||||
Malignant neoplasm of breast
|
0.010 | GeneticVariation | BEFREE | In the present study, rs12075 in DARC and rs2228468 in CCBP2 were genotyped in 806 patients with primary breast cancer. | 30358125 | 2018 |