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rs1863800

From SNPedia

Orientationplus
Stabilizedplus
Make rs1863800(C;C)
Make rs1863800(C;T)
Make rs1863800(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203837937
is asnp
is mentioned by
dbSNPrs1863800
ebirs1863800
HLIrs1863800
Exacrs1863800
Varsomers1863800
Maprs1863800
PheGenIrs1863800
hapmaprs1863800
1000 genomesrs1863800
hgdprs1863800
ensemblrs1863800
gopubmedrs1863800
geneviewrs1863800
scholarrs1863800
googlers1863800
pharmgkbrs1863800
gwascentralrs1863800
openSNPrs1863800
23andMers1863800
23andMe allrs1863800
SNP Nexus

SNPshotrs1863800
SNPdbers1863800
MSV3drs1863800
GWAS Ctlgrs1863800
GMAF0.3577
Max Magnitude

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

[PMID 15022315] Haplotype analysis in simplex families and novel analytic approaches in a case-control cohort reveal no evidence of association of the CTLA-4 gene with rheumatoid arthritis.

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