Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10010325
rs10010325
CUI: C0005890
Disease: Body Height
Body Height
A 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960

2010

dbSNP: rs10010325
rs10010325
CUI: C0021704
Disease: Intelligence
Intelligence
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086

2018

dbSNP: rs10010325
rs10010325
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015

dbSNP: rs10010325
rs10010325
CUI: C0489786
Disease: Height
Height
A 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960

2010

dbSNP: rs10010325
rs10010325
CUI: C0021704
Disease: Intelligence
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs10022109
rs10022109
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs114619974
rs114619974
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic
0.700 GeneticVariation UNIPROT

dbSNP: rs116519313
rs116519313
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic
0.700 GeneticVariation UNIPROT

dbSNP: rs11726786
rs11726786
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694

2017

dbSNP: rs11726786
rs11726786
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs1283441077
rs1283441077
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic
0.700 GeneticVariation UNIPROT

dbSNP: rs1316795626
rs1316795626
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic
0.700 GeneticVariation UNIPROT

dbSNP: rs1391438
rs1391438
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086

2018

dbSNP: rs1391438
rs1391438
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018

dbSNP: rs1391440
rs1391440
CUI: C0021704
Disease: Intelligence
Intelligence
C 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs1391441
rs1391441
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
Malignant neoplasm of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1391441
rs1391441
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019