Source: BEFREE ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16949649
rs16949649
Entrez Id: 4830;654364
Gene Symbol: NME1;NME1-NME2
NME1;NME1-NME2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Patients carrying the C allele in rs16949649 were associated with higher breast cancer-specific mortality [hazard ratio (HR), 1.4; 95% confidence interval (95% CI), 1.1-1.9] compared with those carrying the wild-type allele, and the association was more evident in patients with an early-stage cancer (HR, 1.7; 95% CI, 1.2-2.5). 18676749 2008
dbSNP: rs2302254
rs2302254
Entrez Id: 4830;654364
Gene Symbol: NME1;NME1-NME2
NME1;NME1-NME2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE In vitro biochemical analyses showed that minor alleles in rs2302254 and rs3760468, which is in strong linkage disequilibrium with rs16949646, altered nuclear proteins binding capacity and reduced NME1 promoter activity, supporting the results from an association study of these SNPs with breast cancer survival. 18676749 2008
dbSNP: rs3760468
rs3760468
Entrez Id: 4830;654364
Gene Symbol: NME1;NME1-NME2
NME1;NME1-NME2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE In vitro biochemical analyses showed that minor alleles in rs2302254 and rs3760468, which is in strong linkage disequilibrium with rs16949646, altered nuclear proteins binding capacity and reduced NME1 promoter activity, supporting the results from an association study of these SNPs with breast cancer survival. 18676749 2008