Disease A B C D E F G H I J K L M N O P Q R S T U V W X Y Z [0-9]
Gene A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

FCGR2A

Gene name: info Fc fragment of IgG, low affinity IIa, receptor (CD32)
OMIM ID: 146790
Chromosome location: 1q23.3

Polymorphisms

Disease/PhenotypeMycobacterium tuberculosis, susceptibility to
Reference transcriptNM_001136219.1
DNA Changec.500A>G
A.A. Changep.His167Arg
Exon/Intronexon 4
Variation Typesubstitution
Reference SNPrs1801274
Cases120 pulmonary TB patients
Controls150 healthy controls
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
H134 (55.83%)169 (56.3%)0.9
R106 (44.17%)131 (43.67%)0.9
HH37 (30.83%)49 (32.67%)0.74
HR60 (50.00%)71 (74.33%)0.66
RR23 (19.17%)30 (20.00%)0.86
CommentsNo association was observed between FCGR2A-131H/R polymorphisms and Pulmonary Tuberculosis,
ReferenceSadki K, Lamsyah H, Rueda B, Akil E, Sadak A, Martin J, El Aouad R. Analysis of MIF, FCGR2A and FCGR3A gene polymorphisms with susceptibility to pulmonary tuberculosis in Moroccan population.
J Genet Genomics. 2010 Apr;37(4):257-64.