CSF1, colony stimulating factor 1, 1435

N. diseases: 259; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0392885
Disease:
High density lipoprotein measurement
G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0201899
Disease:
Aspartate aminotransferase measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C2985280
Disease:
Blood Protein Measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0201973
Disease:
Creatine kinase measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0750880
Disease:
Monocyte count result
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0200637
Disease:
Monocyte count procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs333947
rs333947
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0023508
Disease:
White Blood Cell Count procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1058885
rs1058885
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE We investigated the effects of two functional genetic variants, including <i>CSF1</i> rs1058885 and <i>CSF1R</i> rs10079250 in a cohort including 502 Taiwanese patients with PD and 511 age- and gender-matched healthy controls. 31554150 2019
dbSNP: rs2050462
rs2050462
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0007134
Disease:
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE The functional rs2050462 in CSF-1 might have a substantial influence on the renal cell carcinoma susceptibility and evolution in the Chinese population. 29734839 2018
dbSNP: rs2050462
rs2050462
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE The functional rs2050462 in CSF-1 might have a substantial influence on the renal cell carcinoma susceptibility and evolution in the Chinese population. 29734839 2018
dbSNP: rs333951
rs333951
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE However, no statistical significance was found in the association between CSF-1 rs333951 polymorphism and the susceptibility of renal cell carcinoma ( P = 0.589). 29734839 2018
dbSNP: rs333951
rs333951
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0007134
Disease:
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE However, no statistical significance was found in the association between CSF-1 rs333951 polymorphism and the susceptibility of renal cell carcinoma ( P = 0.589). 29734839 2018
dbSNP: rs1058885
rs1058885
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0266929
Disease:
Chronic Periodontitis
0.010 GeneticVariation BEFREE None of the individual SNPs among rs333967, rs2297706, and rs1058885 in CSF-1 was found statistically significantly associated with CP in the Han Chinese population with Shanghai origin, whereas a haplotype T-C-G showed an observed statistically significant association with decreased risk of CP susceptibility in males. 24592910 2014
dbSNP: rs2297706
rs2297706
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0266929
Disease:
Chronic Periodontitis
0.010 GeneticVariation BEFREE None of the individual SNPs among rs333967, rs2297706, and rs1058885 in CSF-1 was found statistically significantly associated with CP in the Han Chinese population with Shanghai origin, whereas a haplotype T-C-G showed an observed statistically significant association with decreased risk of CP susceptibility in males. 24592910 2014
dbSNP: rs333967
rs333967
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C0266929
Disease:
Chronic Periodontitis
0.010 GeneticVariation BEFREE None of the individual SNPs among rs333967, rs2297706, and rs1058885 in CSF-1 was found statistically significantly associated with CP in the Han Chinese population with Shanghai origin, whereas a haplotype T-C-G showed an observed statistically significant association with decreased risk of CP susceptibility in males. 24592910 2014
dbSNP: rs777521033
rs777521033
Entrez Id: 1435
Gene Symbol: CSF1
CSF1
CUI: C2363741
Disease:
HIV-1 infection
0.010 GeneticVariation BEFREE Four SNPs (CCR2-V64I, CCR5-2459, MIP1A+954, and IL2+3896) and specific haplotypes in the IL2 and CCR2/CCR5 regions were significantly associated with HIV-1 infection susceptibility in different genetic models. 16323127 2006