[PMID 24465836] Genetic association of human leukocyte antigens with chronicity or resolution of hepatitis B infection in thai population


[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.


[PMID 25802187] Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B

rs652888

Parent Gene: EHMT2

Importance: 3
Less common allele: G = 21%
More common allele: A = 79%
My Genotype: Log In
Risk Allele: C, G

Disease/Trait: Hepatitis B Infection

rs652888 is associated with Hepatitis B Infection (R) . It is reported to increased association with Chronic hepatitis B infection. No specific risk allele was identified in the study.

Disease/Trait: Membranous Glomerulonephritis

The C allele of rs652888 is reported to be associated with Membranous Glomerulonephritis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Idiopathic membranous nephropathy.

Disease/Trait: Chronic Hepatitis B Infection

The G allele of rs652888 is reported to be associated with Chronic Hepatitis B Infection (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Chronic hepatitis B infection.

Disease/Trait: Drug-Induced Agranulocytosis

rs652888 is associated with Drug-induced Agranulocytosis (R) . It is reported to increased association with Anti-thyroid drug induced agranulocytosis. No specific risk allele was identified in the study.

Disease/Trait: Response To Anti-Thyroid Drug

rs652888 is associated with Response To Anti-thyroid Drug . It is reported to increased association with Anti-thyroid drug induced agranulocytosis. No specific risk allele was identified in the study.