Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2074038
rs2074038
ACCS
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		T 0.700 GeneticVariation GWASCAT Identification of new susceptibility loci for IgA nephropathy in Han Chinese. 26028593

2015
dbSNP: rs35514614
rs35514614
ACCS
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 GeneticVariation UNIPROT

dbSNP: rs376307381
rs376307381
ACCS
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE The impact of three single-nucleotide polymorphisms in eotaxin (SCYA11) gene promoter (-426C>T and -384A>G) and first exon (67G>A) and recently described hexanucleotide (GAAGGA)(n) 10.9 kb upstream on coronary atherosclerosis was investigated. 22773402

2012
dbSNP: rs376307381
rs376307381
ACCS
CUI: C0340288
Disease: Stable angina
Stable angina 		0.010 GeneticVariation BEFREE The GG variant of 67 G>A polymorphism was associated with acute form of CAD compared to stable angina (p=0.0011, p(corr.)=0.013). 22773402

2012