Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16949934
rs16949934
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62103293
rs62103293
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7227892
rs7227892
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs78415359
rs78415359
Entrez Id: 9811;105372107
Gene Symbol: CTIF;LOC105372107
CTIF;LOC105372107
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs41336052
rs41336052
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
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: rs41336052
rs41336052
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
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: rs78415359
rs78415359
Entrez Id: 9811;105372107
Gene Symbol: CTIF;LOC105372107
CTIF;LOC105372107
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12455029
rs12455029
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1317355
rs1317355
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs4939821
rs4939821
Entrez Id: 9811;105372105
Gene Symbol: CTIF;LOC105372105
CTIF;LOC105372105
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs900246
rs900246
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
dbSNP: rs9952724
rs9952724
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657 2006
dbSNP: rs751006365
rs751006365
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.700 GeneticVariation UNIPROT
dbSNP: rs16949646
rs16949646
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0006142
Disease:
Malignant neoplasm of breast 		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: rs16949646
rs16949646
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
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