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rs2069550

From SNPedia

Orientationplus
Stabilizedplus
Make rs2069550(C;C)
Make rs2069550(C;T)
Make rs2069550(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position132888141
GeneTG
is asnp
is mentioned by
dbSNPrs2069550
ebirs2069550
HLIrs2069550
Exacrs2069550
Varsomers2069550
Maprs2069550
PheGenIrs2069550
hapmaprs2069550
1000 genomesrs2069550
hgdprs2069550
ensemblrs2069550
gopubmedrs2069550
geneviewrs2069550
scholarrs2069550
googlers2069550
pharmgkbrs2069550
gwascentralrs2069550
openSNPrs2069550
23andMers2069550
23andMe allrs2069550
SNP Nexus

SNPshotrs2069550
SNPdbers2069550
MSV3drs2069550
GWAS Ctlgrs2069550
GMAF0.3623
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