Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025313
rs869025313
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
0.800 GeneticVariation UNIPROT Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
dbSNP: rs869025314
rs869025314
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
0.800 GeneticVariation UNIPROT Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
dbSNP: rs869025315
rs869025315
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
0.800 GeneticVariation UNIPROT Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
dbSNP: rs869025313
rs869025313
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
G 0.800 CausalMutation CLINVAR
dbSNP: rs869025314
rs869025314
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
T 0.800 CausalMutation CLINVAR
dbSNP: rs869025315
rs869025315
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C4225206
Disease:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
T 0.800 CausalMutation CLINVAR
dbSNP: rs2306272
rs2306272
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs332388
rs332388
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs332388
rs332388
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0007102
Disease:
Malignant tumor of colon
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0009404
Disease:
Colorectal Neoplasms
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C1302401
Disease:
Adenoma of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs6781752
rs6781752
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs7626079
rs7626079
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs145763646
rs145763646
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0006370
Disease:
Bulimia
A 0.700 GeneticVariation GWASCAT Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. 29391396 2018
dbSNP: rs145763646
rs145763646
Entrez Id: 115286
Gene Symbol: SLC25A26
SLC25A26
CUI: C0005586
Disease:
Bipolar Disorder
A 0.700 GeneticVariation GWASCAT Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. 29391396 2018
dbSNP: rs147372871
rs147372871
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs202007714
rs202007714
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs202007714
rs202007714
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0017654
Disease:
Glomerular Filtration Rate
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018