NMI, N-myc and STAT interactor, 9111

N. diseases: 40; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2278089
rs2278089
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs289828
rs289828
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs11730
rs11730
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0017638
Disease:
Glioma 		0.010 GeneticVariation BEFREE Unconditional logistic regression showed that the variant genotypes of rs2278089 [adjusted odds ratio (OR) = 1.57, P = 4.23 × 10(-6)], rs2194492 (adjusted OR = 1.49, P = 1.20 × 10(-4)), and rs6734376 (adjusted OR = 0.06, P = 8.65 × 10(-13)) significantly affected glioma risk compared with the major homozygotes, while the minor homozygotes of rs3854012 (adjusted OR = 0.54, P = 4.64 × 10(-6)) and rs11730 (adjusted OR = 0.60, P = 1.50 × 10(-4)) showed significant protective effects. 25387807 2015
dbSNP: rs2194492
rs2194492
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0017638
Disease:
Glioma 		0.010 GeneticVariation BEFREE Unconditional logistic regression showed that the variant genotypes of rs2278089 [adjusted odds ratio (OR) = 1.57, P = 4.23 × 10(-6)], rs2194492 (adjusted OR = 1.49, P = 1.20 × 10(-4)), and rs6734376 (adjusted OR = 0.06, P = 8.65 × 10(-13)) significantly affected glioma risk compared with the major homozygotes, while the minor homozygotes of rs3854012 (adjusted OR = 0.54, P = 4.64 × 10(-6)) and rs11730 (adjusted OR = 0.60, P = 1.50 × 10(-4)) showed significant protective effects. 25387807 2015
dbSNP: rs2278089
rs2278089
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0017638
Disease:
Glioma 		0.010 GeneticVariation BEFREE Unconditional logistic regression showed that the variant genotypes of rs2278089 [adjusted odds ratio (OR) = 1.57, P = 4.23 × 10(-6)], rs2194492 (adjusted OR = 1.49, P = 1.20 × 10(-4)), and rs6734376 (adjusted OR = 0.06, P = 8.65 × 10(-13)) significantly affected glioma risk compared with the major homozygotes, while the minor homozygotes of rs3854012 (adjusted OR = 0.54, P = 4.64 × 10(-6)) and rs11730 (adjusted OR = 0.60, P = 1.50 × 10(-4)) showed significant protective effects. 25387807 2015
dbSNP: rs3854012
rs3854012
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0017638
Disease:
Glioma 		0.010 GeneticVariation BEFREE Unconditional logistic regression showed that the variant genotypes of rs2278089 [adjusted odds ratio (OR) = 1.57, P = 4.23 × 10(-6)], rs2194492 (adjusted OR = 1.49, P = 1.20 × 10(-4)), and rs6734376 (adjusted OR = 0.06, P = 8.65 × 10(-13)) significantly affected glioma risk compared with the major homozygotes, while the minor homozygotes of rs3854012 (adjusted OR = 0.54, P = 4.64 × 10(-6)) and rs11730 (adjusted OR = 0.60, P = 1.50 × 10(-4)) showed significant protective effects. 25387807 2015
dbSNP: rs6734376
rs6734376
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0017638
Disease:
Glioma 		0.010 GeneticVariation BEFREE Unconditional logistic regression showed that the variant genotypes of rs2278089 [adjusted odds ratio (OR) = 1.57, P = 4.23 × 10(-6)], rs2194492 (adjusted OR = 1.49, P = 1.20 × 10(-4)), and rs6734376 (adjusted OR = 0.06, P = 8.65 × 10(-13)) significantly affected glioma risk compared with the major homozygotes, while the minor homozygotes of rs3854012 (adjusted OR = 0.54, P = 4.64 × 10(-6)) and rs11730 (adjusted OR = 0.60, P = 1.50 × 10(-4)) showed significant protective effects. 25387807 2015
dbSNP: rs11683487
rs11683487
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C0919267
Disease:
ovarian neoplasm 		0.010 GeneticVariation BEFREE For NMI, we identified a SNP (rs11683487) that was associated with a decreased risk of OC (unadjusted P(dominant)=0.004). 19240718 2009
dbSNP: rs11683487
rs11683487
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C1140680
Disease:
Malignant neoplasm of ovary 		0.010 GeneticVariation BEFREE For NMI, we identified a SNP (rs11683487) that was associated with a decreased risk of OC (unadjusted P(dominant)=0.004). 19240718 2009
dbSNP: rs11683487
rs11683487
Entrez Id: 9111
Gene Symbol: NMI
NMI
CUI: C4721610
Disease:
Carcinoma, Ovarian Epithelial 		0.010 GeneticVariation BEFREE For NMI, we identified a SNP (rs11683487) that was associated with a decreased risk of OC (unadjusted P(dominant)=0.004). 19240718 2009