Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41320847
rs41320847
Entrez Id: 57413
Gene Symbol: TMIGD3
TMIGD3
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs41320847
rs41320847
Entrez Id: 57413
Gene Symbol: TMIGD3
TMIGD3
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs9988442
rs9988442
Entrez Id: 5906;57413
Gene Symbol: RAP1A;TMIGD3
RAP1A;TMIGD3
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs746154553
rs746154553
Entrez Id: 140;57413
Gene Symbol: ADORA3;TMIGD3
ADORA3;TMIGD3
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs1544223
rs1544223
Entrez Id: 140;57413
Gene Symbol: ADORA3;TMIGD3
ADORA3;TMIGD3
CUI: C0018802
Disease:
Congestive heart failure 		0.010 GeneticVariation BEFREE Overall, the rs1544223 was significantly associated with CHF risk under the dominant model (<i>P</i> = 0.046, OR = 1.662, 95% CI = 1.009-2.738).But it did not affect disease severity. 29955603 2018
dbSNP: rs35511654
rs35511654
Entrez Id: 140;57413
Gene Symbol: ADORA3;TMIGD3
ADORA3;TMIGD3
CUI: C1956346
Disease:
Coronary Artery Disease 		0.010 GeneticVariation BEFREE A nonsynonymous variant I248L of the adenosine A3 receptor is associated with coronary heart disease in a Latvian population. 21675873 2011
dbSNP: rs35511654
rs35511654
Entrez Id: 140;57413
Gene Symbol: ADORA3;TMIGD3
ADORA3;TMIGD3
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE A nonsynonymous variant I248L of the adenosine A3 receptor is associated with coronary heart disease in a Latvian population. 21675873 2011
dbSNP: rs35511654
rs35511654
Entrez Id: 140;57413
Gene Symbol: ADORA3;TMIGD3
ADORA3;TMIGD3
CUI: C0010068
Disease:
Coronary heart disease 		0.010 GeneticVariation BEFREE We observed a significantly decreased frequency of the rs35511654 C allele in a group of CHD patients compared with that in controls (p = 0.009). 21675873 2011