Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7204230
rs7204230
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0337428
Disease:
Fibrinogen assay
T 0.800 GeneticVariation GWASCAT Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs7204230
rs7204230
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0337428
Disease:
Fibrinogen assay
T 0.800 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs7186520
rs7186520
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7203398
rs7203398
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs12598049
rs12598049
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0337428
Disease:
Fibrinogen assay
0.700 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs6499550
rs6499550
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0337428
Disease:
Fibrinogen assay
0.700 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs11859517
rs11859517
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C0337428
Disease:
Fibrinogen assay
T 0.700 GeneticVariation GWASCAT A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. 26561523 2016
dbSNP: rs7204230
rs7204230
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C1561955
Disease:
Fibrinogen, CTCAE
T 0.700 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs7204230
rs7204230
Entrez Id: 80205
Gene Symbol: CHD9
CHD9
CUI: C1325327
Disease:
fibrinogen activity
T 0.700 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013