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rs2239610

From SNPedia

Orientationplus
Stabilizedplus
Make rs2239610(C;C)
Make rs2239610(C;G)
Make rs2239610(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position80955913
GeneTSHR
is asnp
is mentioned by
dbSNPrs2239610
ebirs2239610
HLIrs2239610
Exacrs2239610
Varsomers2239610
Maprs2239610
PheGenIrs2239610
hapmaprs2239610
1000 genomesrs2239610
hgdprs2239610
ensemblrs2239610
gopubmedrs2239610
geneviewrs2239610
scholarrs2239610
googlers2239610
pharmgkbrs2239610
gwascentralrs2239610
openSNPrs2239610
23andMers2239610
23andMe allrs2239610
SNP Nexus

SNPshotrs2239610
SNPdbers2239610
MSV3drs2239610
GWAS Ctlgrs2239610
GMAF0.2163
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease