FCRL5, Fc receptor like 5, 83416

N. diseases: 22; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17416676
rs17416676
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs3811035
rs3811035
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs3845586
rs3845586
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs6696309
rs6696309
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs6692977
rs6692977
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C2607914
Disease:
Allergic rhinitis (disorder)
0.010 GeneticVariation BEFREE Our results showed that the frequencies of the rs6692977 CT genotype and T allele within FCRL5 were significantly higher in asthma with comorbid AR compared to healthy controls (Bonferroni-corrected p (Pc) = 3.75 × 10<sup>-6</sup>; Pc = 0.006, respectively), whereas these of the CC genotype and C allele were significantly lower (Pc = 4.15 × 10<sup>-5</sup>; Pc = 0.006, respectively). 30771554 2019
dbSNP: rs6692977
rs6692977
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE Our results showed that the frequencies of the rs6692977 CT genotype and T allele within FCRL5 were significantly higher in asthma with comorbid AR compared to healthy controls (Bonferroni-corrected p (Pc) = 3.75 × 10<sup>-6</sup>; Pc = 0.006, respectively), whereas these of the CC genotype and C allele were significantly lower (Pc = 4.15 × 10<sup>-5</sup>; Pc = 0.006, respectively). 30771554 2019
dbSNP: rs1365504296
rs1365504296
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE This is the first study demonstrating that the APOE*E2 allele modifies the natural history of AD typified by the age of onset in E280A mutation carriers. 26619808 2016
dbSNP: rs3811035
rs3811035
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Three of the FCRL5 tag SNPs, rs6667109, rs3811035 and rs6692977 showed association with GD (P = 0·015-0·001, OR = 1·15-1·16). 20626413 2010
dbSNP: rs6667109
rs6667109
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Three of the FCRL5 tag SNPs, rs6667109, rs3811035 and rs6692977 showed association with GD (P = 0·015-0·001, OR = 1·15-1·16). 20626413 2010
dbSNP: rs6692977
rs6692977
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE Three of the FCRL5 tag SNPs, rs6667109, rs3811035 and rs6692977 showed association with GD (P = 0·015-0·001, OR = 1·15-1·16). 20626413 2010
dbSNP: rs12036228
rs12036228
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0038013
Disease:
Ankylosing spondylitis
0.010 GeneticVariation BEFREE Our results show that in addition to B27, the SNPs rs6427384 and rs12036228 were associated with AS, and the C-T haplotype was higher in cases with AS than in the control population [74.8% vs 63.6%, Fisher's P = 0.003, odds ratio (OR) = 1.660,95% confidence interval (CI) = 1.184-- 2.326]. 19775371 2009
dbSNP: rs6427384
rs6427384
Entrez Id: 83416
Gene Symbol: FCRL5
FCRL5
CUI: C0038013
Disease:
Ankylosing spondylitis
0.010 GeneticVariation BEFREE Our results show that in addition to B27, the SNPs rs6427384 and rs12036228 were associated with AS, and the C-T haplotype was higher in cases with AS than in the control population [74.8% vs 63.6%, Fisher's P = 0.003, odds ratio (OR) = 1.660,95% confidence interval (CI) = 1.184-- 2.326]. 19775371 2009