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rs9355610

From SNPedia

Orientationplus
Stabilizedplus
Make rs9355610(A;A)
Make rs9355610(A;G)
Make rs9355610(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position166969587
is asnp
is mentioned by
dbSNPrs9355610
ebirs9355610
HLIrs9355610
Exacrs9355610
Varsomers9355610
Maprs9355610
PheGenIrs9355610
hapmaprs9355610
1000 genomesrs9355610
hgdprs9355610
ensemblrs9355610
gopubmedrs9355610
geneviewrs9355610
scholarrs9355610
googlers9355610
pharmgkbrs9355610
gwascentralrs9355610
openSNPrs9355610
23andMers9355610
23andMe allrs9355610
SNP Nexus

SNPshotrs9355610
SNPdbers9355610
MSV3drs9355610
GWAS Ctlgrs9355610
GMAF0.4426
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21841780]
Trait
Title A genome-wide association study identifies two new risk loci for Graves' disease.
Risk Allele G
P-val 7E-10
Odds Ratio 1.1900 [1.13-1.26]


[PMID 22489947] The replication of the association of the rs6832151 within chromosomal band 4p14 with Graves' disease in a Polish Caucasian population.


[PMID 22922229OA-icon.png] Seven newly identified loci for autoimmune thyroid disease.


[PMID 25928629OA-icon.png] RNASET2 tag SNP but not CCR6 polymorphisms is associated with autoimmune thyroid diseases in the Chinese Han population