ZNF208, zinc finger protein 208, 7757

N. diseases: 11; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2188971
rs2188971
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Statistical results showed that three variants were associated with the risk of ischemic stroke under allele models (rs2188971, rs2188972, rs8103163 and rs7248488). 27936511 2017
dbSNP: rs2188971
rs2188971
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE We also found that three SNPS in ZNF208 associated with CAD, respectively, rs2188971, rs8103163 and rs7248488.Linkage disequilibrium (LD) and haplotype analyses of the SNPs found that the CTA haplotype (rs1056675, rs1056654, rs11859599) and rs2188972A/rs2188971T/rs8103163A/rs7248488A (ATAA) were associated with CAD. 29100383 2017
dbSNP: rs2188972
rs2188972
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE The variant rs2188972 was also associated with the risk of ischemic stroke in a recessive model after adjustment for age and sex. 27936511 2017
dbSNP: rs7248488
rs7248488
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Statistical results showed that three variants were associated with the risk of ischemic stroke under allele models (rs2188971, rs2188972, rs8103163 and rs7248488). 27936511 2017
dbSNP: rs7248488
rs7248488
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE We also found that three SNPS in ZNF208 associated with CAD, respectively, rs2188971, rs8103163 and rs7248488.Linkage disequilibrium (LD) and haplotype analyses of the SNPs found that the CTA haplotype (rs1056675, rs1056654, rs11859599) and rs2188972A/rs2188971T/rs8103163A/rs7248488A (ATAA) were associated with CAD. 29100383 2017
dbSNP: rs8103163
rs8103163
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE We also found that three SNPS in ZNF208 associated with CAD, respectively, rs2188971, rs8103163 and rs7248488.Linkage disequilibrium (LD) and haplotype analyses of the SNPs found that the CTA haplotype (rs1056675, rs1056654, rs11859599) and rs2188972A/rs2188971T/rs8103163A/rs7248488A (ATAA) were associated with CAD. 29100383 2017
dbSNP: rs7248488
rs7248488
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0152018
Disease:
Esophageal carcinoma
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016
dbSNP: rs7248488
rs7248488
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016
dbSNP: rs7248488
rs7248488
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0546837
Disease:
Malignant neoplasm of esophagus
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016
dbSNP: rs8103163
rs8103163
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0546837
Disease:
Malignant neoplasm of esophagus
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016
dbSNP: rs8103163
rs8103163
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016
dbSNP: rs8103163
rs8103163
Entrez Id: 7757
Gene Symbol: ZNF208
ZNF208
CUI: C0152018
Disease:
Esophageal carcinoma
0.010 GeneticVariation BEFREE Logistic regressionl analysis showed that two SNPs (rs8103163 and rs7248488) were associated with an increased risk of esophageal cancer under different inheritance models after Bonferroni correction. 27907911 2016