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rs11571297

From SNPedia

Orientationminus
Stabilizedminus
Make rs11571297(A;A)
Make rs11571297(A;G)
Make rs11571297(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position203880280
is asnp
is mentioned by
dbSNPrs11571297
ebirs11571297
HLIrs11571297
Exacrs11571297
Varsomers11571297
Maprs11571297
PheGenIrs11571297
hapmaprs11571297
1000 genomesrs11571297
hgdprs11571297
ensemblrs11571297
gopubmedrs11571297
geneviewrs11571297
scholarrs11571297
googlers11571297
pharmgkbrs11571297
gwascentralrs11571297
openSNPrs11571297
23andMers11571297
23andMe allrs11571297
SNP Nexus

SNPshotrs11571297
SNPdbers11571297
MSV3drs11571297
GWAS Ctlgrs11571297
GMAF0.3898
Max Magnitude

[PMID 19175525OA-icon.png] CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data

[PMID 20537165OA-icon.png] The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease


[PMID 18200060] PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not.


[PMID 18292987OA-icon.png] Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes.


[PMID 19622768OA-icon.png] CTLA4 variants, UV-induced tolerance, and risk of non-melanoma skin cancer.


[PMID 19672595OA-icon.png] Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?