TBC1D9, TBC1 domain family member 9, 23158

N. diseases: 491; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12386422
rs12386422
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs12386428
rs12386428
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs12500421
rs12500421
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs17006401
rs17006401
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6835008
rs6835008
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6844563
rs6844563
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6853171
rs6853171
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6853487
rs6853487
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7659321
rs7659321
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1452199941
rs1452199941
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE Our data showed that the risk for lung cancer increased significantly among the variant Arg194Trp (C > T, rs1799782) and Arg399Gln (G > A, rs25487) of XRCC1, but there are no significant differences in the allelic and genotypic frequencies of c.1564A > T and c.3073A > C of MDR1 between lung cancer patients and cancer-free controls. 25563194 2015
dbSNP: rs1452199941
rs1452199941
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE Our data showed that the risk for lung cancer increased significantly among the variant Arg194Trp (C > T, rs1799782) and Arg399Gln (G > A, rs25487) of XRCC1, but there are no significant differences in the allelic and genotypic frequencies of c.1564A > T and c.3073A > C of MDR1 between lung cancer patients and cancer-free controls. 25563194 2015
dbSNP: rs1452199941
rs1452199941
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE Our data showed that the risk for lung cancer increased significantly among the variant Arg194Trp (C > T, rs1799782) and Arg399Gln (G > A, rs25487) of XRCC1, but there are no significant differences in the allelic and genotypic frequencies of c.1564A > T and c.3073A > C of MDR1 between lung cancer patients and cancer-free controls. 25563194 2015
dbSNP: rs965468440
rs965468440
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C1096063
Disease:
Drug Resistant Epilepsy
0.010 GeneticVariation BEFREE The obtained results clearly confirm the lack of a connection between the occurrence of drug-resistant epilepsy and C435T polymorphism of the MDR1 gene irrespective of the definition of drug resistance applied to the patient. 25223475 2014
dbSNP: rs1452199941
rs1452199941
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE The purpose of this study is to compare the genotype frequency of C3435T and G1199A polymorphisms in MDR1 between ESRD patients and healthy controls in the Chinese population to determine whether the alteration of the P-gp function is associated with ESRD. 17376299 2007
dbSNP: rs1452199941
rs1452199941
Entrez Id: 23158
Gene Symbol: TBC1D9
TBC1D9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE The purpose of this study is to compare the genotype frequency of C3435T and G1199A polymorphisms in MDR1 between ESRD patients and healthy controls in the Chinese population to determine whether the alteration of the P-gp function is associated with ESRD. 17376299 2007