Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0007102
Disease:
Malignant tumor of colon 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0009402
Disease:
Colorectal Carcinoma 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs77776598
rs77776598
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0009404
Disease:
Colorectal Neoplasms 		C 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0007102
Disease:
Malignant tumor of colon 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C1302401
Disease:
Adenoma of large intestine 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs78368589
rs78368589
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs7447815
rs7447815
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0027051
Disease:
Myocardial Infarction 		0.010 GeneticVariation BEFREE The frequency of the T-C haplotype (rs7728646-rs7447815) was significantly higher for the M</span>I patients when compared with controls (P=0.037). 21420947 2011
dbSNP: rs7447815
rs7447815
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE A nonsense polymorphism (Y319X) of the solute carrier family 6 member 18 (SLC6A18) gene is not associated with hypertension and blood pressure in Japanese. 16340170 2006