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rs2184658

From SNPedia

Orientationplus
Stabilizedplus
Make rs2184658(C;C)
Make rs2184658(C;G)
Make rs2184658(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position220879115
GeneHLX
is asnp
is mentioned by
dbSNPrs2184658
ebirs2184658
HLIrs2184658
Exacrs2184658
Varsomers2184658
Maprs2184658
PheGenIrs2184658
hapmaprs2184658
1000 genomesrs2184658
hgdprs2184658
ensemblrs2184658
gopubmedrs2184658
geneviewrs2184658
scholarrs2184658
googlers2184658
pharmgkbrs2184658
gwascentralrs2184658
openSNPrs2184658
23andMers2184658
23andMe allrs2184658
SNP Nexus

SNPshotrs2184658
SNPdbers2184658
MSV3drs2184658
GWAS Ctlgrs2184658
GMAF0.1593
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22014209] Functional polymorphisms in TBX21 and HLX are associated with development and prognosis of Graves' disease