Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10405178
rs10405178
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10405178
rs10405178
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0154723
Disease:
Migraine with Aura 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4022761
Disease:
Reduced brain N-acetyl aspartate level by MRS 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C1843156
Disease:
Progressive sensorineural hearing impairment 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C1844917
Disease:
Intermittent lactic acidemia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C3806347
Disease:
Hyperhomocystinemia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0027498
Disease:
Nausea and vomiting 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0268070
Disease:
Hypocupremia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4025360
Disease:
Functional motor deficit 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C1609528
Disease:
Restrictive deficit on pulmonary function testing 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0241657
Disease:
Abnormality of the vasculature 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4025729
Disease:
Neuromuscular dysphagia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C1850830
Disease:
Exercise-induced myalgia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0086769
Disease:
Panic Attacks 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4022160
Disease:
Motheaten muscle fibers 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0042870
Disease:
Vitamin D Deficiency 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0240997
Disease:
Decreased serum ceruloplasmin 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0041105
Disease:
Trismus 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C4476567
Disease:
Reduced brain choline level by MRS 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C1849489
Disease:
Increased serum alanine 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1568523935
rs1568523935
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0878544
Disease:
Cardiomyopathies 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs864321624
rs864321624
Entrez Id: 284439
Gene Symbol: SLC25A42
SLC25A42
CUI: C0162670
Disease:
Mitochondrial Myopathies 		G 0.700 GeneticVariation CLINVAR