Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10511323
rs10511323
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12631733
rs12631733
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C1302401
Disease:
Adenoma of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0009404
Disease:
Colorectal Neoplasms 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0007102
Disease:
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs72942485
rs72942485
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs73235136
rs73235136
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091 2019
dbSNP: rs73235136
rs73235136
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. 31417091 2019
dbSNP: rs73235147
rs73235147
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs3814399
rs3814399
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0264408
Disease:
Childhood asthma 		0.700 GeneticVariation GWASDB Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. 23829686 2013
dbSNP: rs367589886
rs367589886
Entrez Id: 91653
Gene Symbol: BOC
BOC
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.700 GeneticVariation UNIPROT