rs11571297

Orientation

minus

Stabilized

minus

Make rs11571297(A;A)

Make rs11571297(A;G)

Make rs11571297(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

203880280

is a	snp
is	mentioned by
dbSNP	rs11571297
dbSNP (classic)	rs11571297
ClinGen	rs11571297
ebi	rs11571297
HLI	rs11571297
Exac	rs11571297
Gnomad	rs11571297
Varsome	rs11571297
LitVar	rs11571297
Map	rs11571297
PheGenI	rs11571297
Biobank	rs11571297
1000 genomes	rs11571297
hgdp	rs11571297
ensembl	rs11571297
geneview	rs11571297
scholar	rs11571297
google	rs11571297
pharmgkb	rs11571297
gwascentral	rs11571297
openSNP	rs11571297
23andMe	rs11571297
SNPshot	rs11571297
SNPdbe	rs11571297
MSV3d	rs11571297
GWAS Ctlg	rs11571297

GMAF

0.3898

Max Magnitude

0

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

[PMID 20537165] 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 18292987] Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes.

[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?