Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35215132
rs35215132
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8003014
rs8003014
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs10133673
rs10133673
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0008924
Disease:
Cleft upper lip 		G 0.700 GeneticVariation GWASCAT Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. 28232668 2017
dbSNP: rs10133673
rs10133673
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0008925
Disease:
Cleft Palate 		G 0.700 GeneticVariation GWASCAT Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. 28232668 2017
dbSNP: rs848087
rs848087
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0678222
Disease:
Breast Carcinoma 		G 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs2144319
rs2144319
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0428474
Disease:
Serum LDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs2144319
rs2144319
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1389068504
rs1389068504
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0026847
Disease:
Spinal Muscular Atrophy 		0.010 GeneticVariation BEFREE The patient carries a homozygous pathogenic variant c.695A>G; p.(Lys232Arg) in the SLC25A21 gene, encoding the mitochondrial oxodicarboxylate carrier, and developed spinal muscular atrophy and mitochondrial myopathy. 29517768 2018
dbSNP: rs1389068504
rs1389068504
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0162670
Disease:
Mitochondrial Myopathies 		0.010 GeneticVariation BEFREE The patient carries a homozygous pathogenic variant c.695A>G; p.(Lys232Arg) in the SLC25A21 gene, encoding the mitochondrial oxodicarboxylate carrier, and developed spinal muscular atrophy and mitochondrial myopathy. 29517768 2018
dbSNP: rs764622508
rs764622508
Entrez Id: 89874
Gene Symbol: SLC25A21
SLC25A21
CUI: C0027651
Disease:
Neoplasms 		0.010 GeneticVariation BEFREE Previous research suggests that the G315A single-nucleotide polymorphism in the ornithine decarboxylase (ODC) gene may be a genetic marker for risk of colorectal neoplasia and may also modify the association of aspirin use with risk. 17047198 2006