Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs59490629
rs59490629
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs59490629
rs59490629
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C1611184
Disease:
Calcification of coronary artery
0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs9486594
rs9486594
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease. 25514360 2015
dbSNP: rs61315837
rs61315837
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs7772518
rs7772518
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
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: rs118203955
rs118203955
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C3553358
Disease:
COENZYME Q10 DEFICIENCY, PRIMARY, 3
A 0.700 CausalMutation CLINVAR Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. 17374725 2007
dbSNP: rs118203956
rs118203956
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C3553358
Disease:
COENZYME Q10 DEFICIENCY, PRIMARY, 3
A 0.700 CausalMutation CLINVAR Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. 17374725 2007
dbSNP: rs782439454
rs782439454
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
CUI: C3553358
Disease:
COENZYME Q10 DEFICIENCY, PRIMARY, 3
A 0.700 GeneticVariation CLINVAR