MX1, MX dynamin like GTPase 1, 4599

N. diseases: 71; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17000900
rs17000900
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0026769
Disease:
Multiple Sclerosis
0.020 GeneticVariation BEFREE In the present case-control study, we evaluated the association between three SNPs at nt -123 (A or C, rs17000900), nt -88 (G or T, rs2071430), and nt +20 (A or C, rs464138) and MS risk as well as treatment response in a population of Iranian MS patients including 146 IFNβ responders and 85 non-responders as well as 180 healthy controls. 28386647 2017
dbSNP: rs17000900
rs17000900
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0026769
Disease:
Multiple Sclerosis
0.020 GeneticVariation BEFREE The objective of this study was to evaluate the associations between two MXA promoter region single nucleotide polymorphisms (rs2071430 and rs17000900) and the gene expression responses, clinical and MRI phenotypes in IFN-beta treated MS patients. 17126411 2007
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0019196
Disease:
Hepatitis C
0.010 GeneticVariation BEFREE Patients with MxA rs2071430 TT genotype were more likely to develop HCV infection chronicity (additive model: odds ratio (OR) 1.22, 95% confidence interval (CI) 1.01-1.48, P = 0.042). 29271328 2018
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE In the present case-control study, we evaluated the association between three SNPs at nt -123 (A or C, rs17000900), nt -88 (G or T, rs2071430), and nt +20 (A or C, rs464138) and MS risk as well as treatment response in a population of Iranian MS patients including 146 IFNβ responders and 85 non-responders as well as 180 healthy controls. 28386647 2017
dbSNP: rs464138
rs464138
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE In the present case-control study, we evaluated the association between three SNPs at nt -123 (A or C, rs17000900), nt -88 (G or T, rs2071430), and nt +20 (A or C, rs464138) and MS risk as well as treatment response in a population of Iranian MS patients including 146 IFNβ responders and 85 non-responders as well as 180 healthy controls. 28386647 2017
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE Influence of MX1 promoter rs2071430 G/T polymorphism on susceptibility to systemic lupus erythematosus. 26815367 2016
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE MxA SNP rs2071430 GG genotype is significantly associated with prostate cancer irrespective of race. 23438650 2013
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0600139
Disease:
Prostate carcinoma
0.010 GeneticVariation BEFREE MxA SNP rs2071430 GG genotype is significantly associated with prostate cancer irrespective of race. 23438650 2013
dbSNP: rs17000900
rs17000900
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE Our result showed rs17000900 (MxA-123) and rs461093 were significantly associated with the risk of AD. 22950423 2012
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0234985
Disease:
Mental deterioration
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs2071430
rs2071430
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0338656
Disease:
Impaired cognition
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs457274
rs457274
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0234985
Disease:
Mental deterioration
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs457274
rs457274
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0338656
Disease:
Impaired cognition
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs461093
rs461093
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE Our result showed rs17000900 (MxA-123) and rs461093 were significantly associated with the risk of AD. 22950423 2012
dbSNP: rs469083
rs469083
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0338656
Disease:
Impaired cognition
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs469083
rs469083
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0234985
Disease:
Mental deterioration
0.010 GeneticVariation BEFREE The carriers of minor alleles of five MxA SNPs, including rs457274, rs2071430 (MxA -88), rs461093, rs469083, and rs1557372, were associated with faster cognitive decline over 2 years. 22950423 2012
dbSNP: rs763554423
rs763554423
Entrez Id: 4599
Gene Symbol: MX1
MX1
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE The association with the susceptibility to HBV infection was only observed for IL10RB K47E when we compared the individuals with persistent HBV infection through nonmaternal transmission to the controls with asymptomatic self-limited HBV infection. 19714778 2009