Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28358278
rs28358278
Entrez Id: 4514;4537;4538;4539;4540
Gene Symbol: COX3;ND3;ND4;ND4L;ND5
COX3;ND3;ND4;ND4L;ND5
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE In stratified analysis, rs28358278, rs2853826, and rs41467651 were associated with subgroups of GC, with the rs28358278 G, rs2853826 T, and rs41467651 T alleles associated with an increased GC risk in females (adjusted OR = 1.70, 95% CI = 1.08-2.69, <i>P</i> = 0.023; adjusted OR = 1.78, 95% CI = 1.11-2.85, <i>P</i> = 0.016; adjusted OR = 2.07, 95% CI = 1.04-4.12, <i>P</i> = 0.038, respectively). 30275759 2018
dbSNP: rs2853826
rs2853826
Entrez Id: 4514;4537;4538;4539;4540
Gene Symbol: COX3;ND3;ND4;ND4L;ND5
COX3;ND3;ND4;ND4L;ND5
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE In stratified analysis, rs28358278, rs2853826</span>, and rs41467651 were associated with subgroups of GC, with the rs28358278 G, rs2853826</span> T, and rs41467651 T alleles associated with an increased GC risk in females (adjusted OR = 1.70, 95% CI = 1.08-2.69, <i>P</i> = 0.023; adjusted OR = 1.78, 95% CI = 1.11-2.85, <i>P</i> = 0.016; adjusted OR = 2.07, 95% CI = 1.04-4.12, <i>P</i> = 0.038, respectively). 30275759 2018
dbSNP: rs41467651
rs41467651
Entrez Id: 4514;4537;4538;4539
Gene Symbol: COX3;ND3;ND4;ND4L
COX3;ND3;ND4;ND4L
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE In stratified analysis, rs28358278, rs2853826, and rs41467651</span> were associated with subgroups of GC, with the rs28358278 G, rs2853826 T, and rs41467651 T alleles associated with an increased GC risk in females (adjusted OR = 1.70, 95% CI = 1.08-2.69, <i>P</i> = 0.023; adjusted OR = 1.78, 95% CI = 1.11-2.85, <i>P</i> = 0.016; adjusted OR = 2.07, 95% CI = 1.04-4.12, <i>P</i> = 0.038, respectively). 30275759 2018