FCER2, Fc fragment of IgE receptor II, 2208

N. diseases: 104; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113893384
rs113893384
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs12973524
rs12973524
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2277989
rs2277989
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs7246264
rs7246264
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7246264
rs7246264
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7249360
rs7249360
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs28364072
rs28364072
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0004096
Disease:
Asthma 		0.010 GeneticVariation BEFREE This study aims to investigate the association of genetic variations: rs28364072 and rs7249320 with asthma and its severity in north Indian children. 24102092 2013
dbSNP: rs7249320
rs7249320
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0004096
Disease:
Asthma 		0.010 GeneticVariation BEFREE This study aims to investigate the association of genetic variations: rs28364072 and rs7249320 with asthma and its severity in north Indian children. 24102092 2013
dbSNP: rs2228137
rs2228137
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0004096
Disease:
Asthma 		0.010 GeneticVariation BEFREE A SNP (rs2228137) (R62W) in FCER2 has been linked with severe exacerbations in asthmatics. 22059556 2011
dbSNP: rs2228137
rs2228137
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0004096
Disease:
Asthma 		0.010 GeneticVariation BEFREE A SNP (rs2228137) (R62W) in FCER2 has been linked with severe exacerbations in asthmatics. 22059556 2011
dbSNP: rs34694289
rs34694289
Entrez Id: 2208
Gene Symbol: FCER2
FCER2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.010 GeneticVariation BEFREE In the second approach, we typed four nonsynonymous polymorphisms in genes C3 (R102G and L314P) and ICAM1 (G241R and K469E) in four independent cohorts totaling 2178 IBD cases. 16570073 2006