[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease


[PMID 21040781] CTLA-4 confers a risk of recurrent schizophrenia, major depressive disorder and bipolar disorder in the Chinese Han population


[PMID 19300490] An African ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in African Americans.


[PMID 19956097] Remapping the type I diabetes association of the CTLA4 locus.


[PMID 19956101] Overview of the Rapid Response data.


[PMID 19956106] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.


[PMID 20352109] Association of the CTLA4 gene with Graves' disease in the Chinese Han population.


[PMID 22977635] Association study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population

rs231779

Parent Gene: CTLA4

Importance: 3
Less common allele: T = 44%
More common allele: C = 56%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Hypothyroidism

The T allele of rs231779 is reported to be associated with Hypothyroidism (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Hypothyroidism.