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rs231779

From SNPedia

Orientationplus
Stabilizedplus
Make rs231779(C;C)
Make rs231779(C;T)
Make rs231779(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203869764
GeneCTLA4
is asnp
is mentioned by
dbSNPrs231779
ebirs231779
HLIrs231779
Exacrs231779
Varsomers231779
Maprs231779
PheGenIrs231779
hapmaprs231779
1000 genomesrs231779
hgdprs231779
ensemblrs231779
gopubmedrs231779
geneviewrs231779
scholarrs231779
googlers231779
pharmgkbrs231779
gwascentralrs231779
openSNPrs231779
23andMers231779
23andMe allrs231779
SNP Nexus

SNPshotrs231779
SNPdbers231779
MSV3drs231779
GWAS Ctlgrs231779
GMAF0.4738
Max Magnitude
? (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

GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele T
P-val 0.000007
Odds Ratio 1.1260 None


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


[PMID 19956097OA-icon.png] Remapping the type I diabetes association of the CTLA4 locus.


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


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


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


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


[PMID 27888068] Associations of single nucleotide polymorphisms of PTPN22 and Ctla4 genes with the risk of allergic rhinitis in a Chinese Han population.