NIN, ninein, 51199

N. diseases: 52; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61755581
rs61755581
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0678222
Disease:
Breast Carcinoma 		0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463 2019
dbSNP: rs72681698
rs72681698
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs72681698
rs72681698
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs146291102
rs146291102
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs8012283
rs8012283
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0024143
Disease:
Lupus Nephritis 		G 0.700 GeneticVariation GWASCAT Lupus nephritis susceptibility loci in women with systemic lupus erythematosus. 24925725 2014
dbSNP: rs8012283
rs8012283
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		G 0.700 GeneticVariation GWASCAT Lupus nephritis susceptibility loci in women with systemic lupus erythematosus. 24925725 2014
dbSNP: rs387907308
rs387907308
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C3553870
Disease:
SECKEL SYNDROME 7 		C 0.700 CausalMutation CLINVAR
dbSNP: rs747680111
rs747680111
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C3553870
Disease:
SECKEL SYNDROME 7 		C 0.700 CausalMutation CLINVAR
dbSNP: rs10145182
rs10145182
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE A two SNP combination of rs10145182 in NIN and rs2134808 in the TUBG1 locus (P-interaction = 0.00001), suggested SNPs in mediators of microtubule nucleation from the centrosome contribute to breast cancer. 20508983 2011
dbSNP: rs10145182
rs10145182
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE A two SNP combination of rs10145182 in NIN and rs2134808 in the TUBG1 locus (P-interaction = 0.00001), suggested SNPs in mediators of microtubule nucleation from the centrosome contribute to breast cancer. 20508983 2011