Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.320 GeneticVariation group BEFREE Analysis of VNTRs in the solute carrier family 6, member 18 (SLC6A18) and lack of association with hypertension. 18554081 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.320 GeneticVariation group BEFREE This is the first report showing that a single polymorphism in SLC6A18 is not associated with hypertension or blood pressure in Japanese. 16340170 2006
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.320 Biomarker group CTD_human Hypertension and impaired glycine handling in mice lacking the orphan transporter XT2. 15121838 2004
CUI: C0268654
Disease: Iminoglycinuria
Iminoglycinuria
0.310 Biomarker disease BEFREE Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes. 19033659 2008
CUI: C0268654
Disease: Iminoglycinuria
Iminoglycinuria
0.310 GeneticVariation disease ORPHANET Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes. 19033659 2008
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.100 GeneticVariation group GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.100 GeneticVariation group GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
Malignant neoplasm of large intestine
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
Malignant neoplasm of large intestine
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.100 GeneticVariation phenotype GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.100 GeneticVariation phenotype GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.100 GeneticVariation disease GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.100 GeneticVariation disease GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 GeneticVariation disease BEFREE These results suggest that SLC6A18 or neighboring genes are associated with increased susceptibility to MI. 21420947 2011