rs231777
| Orientation | plus |
| Stabilized | plus |
| Make rs231777(C;C) |
| Make rs231777(C;T) |
| Make rs231777(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 203868865 |
| Gene | CTLA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs231777 |
| dbSNP (classic) | rs231777 |
| ClinGen | rs231777 |
| ebi | rs231777 |
| HLI | rs231777 |
| Exac | rs231777 |
| Gnomad | rs231777 |
| Varsome | rs231777 |
| LitVar | rs231777 |
| Map | rs231777 |
| PheGenI | rs231777 |
| Biobank | rs231777 |
| 1000 genomes | rs231777 |
| hgdp | rs231777 |
| ensembl | rs231777 |
| geneview | rs231777 |
| scholar | rs231777 |
| rs231777 | |
| pharmgkb | rs231777 |
| gwascentral | rs231777 |
| openSNP | rs231777 |
| 23andMe | rs231777 |
| SNPshot | rs231777 |
| SNPdbe | rs231777 |
| MSV3d | rs231777 |
| GWAS Ctlg | rs231777 |
| GMAF | 0.1529 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[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 18773895
] The genetic basis of primary biliary cirrhosis: premises, not promises.
[PMID 18778710] Primary biliary cirrhosis is associated with a genetic variant in the 3' flanking region of the CTLA4 gene.
[PMID 19300490] An African ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in African Americans.
[PMID 19609446] CTLA4 autoimmunity-associated genotype contributes to severe pulmonary tuberculosis in an African population.
[PMID 19622768] CTLA4 variants, UV-induced tolerance, and risk of non-melanoma skin cancer.
[PMID 19672595] Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?
[PMID 19956097] Remapping the type I diabetes association of the CTLA4 locus.
[PMID 19956101] Overview of the Rapid Response data.
[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
[PMID 30223781] Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population.
