NREP, neuronal regeneration related protein, 9315

N. diseases: 40; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs141344917
rs141344917
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3797737
rs3797737
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56084922
rs56084922
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs57201028
rs57201028
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs79692389
rs79692389
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs980888
rs980888
Entrez Id: 9315;100873948
Gene Symbol: NREP;NREP-AS1
NREP;NREP-AS1
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1145123
rs1145123
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs154081
rs154081
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs255892
rs255892
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs255896
rs255896
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs27757
rs27757
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs3797733
rs3797733
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs3797733
rs3797733
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs56084922
rs56084922
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs56116444
rs56116444
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0032181
Disease:
Platelet Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7722878
rs7722878
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7722878
rs7722878
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs6882649
rs6882649
Entrez Id: 9315
Gene Symbol: NREP
NREP
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs59739601
rs59739601
Entrez Id: 9315;100505678
Gene Symbol: NREP;STARD4-AS1
NREP;STARD4-AS1
CUI: C0032181
Disease:
Platelet Count measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs613827
rs613827
Entrez Id: 9315;100873948
Gene Symbol: NREP;NREP-AS1
NREP;NREP-AS1
CUI: C4699184
Disease:
Fuchs 		0.010 GeneticVariation BEFREE In the present study, we screened several reported SNPs (rs2286812, rs17595731 and rs613827 in TCF4; rs7640737 and rs2292245 in PTPRG) in FED and non-Fuchs' patients with corneal dystrophies of southern Chinese. 23758498 2014