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rs4889009

From SNPedia

Orientationplus
Stabilizedplus
Make rs4889009(C;C)
Make rs4889009(C;G)
Make rs4889009(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position79666550
is asnp
is mentioned by
dbSNPrs4889009
ebirs4889009
HLIrs4889009
Exacrs4889009
Varsomers4889009
Maprs4889009
PheGenIrs4889009
hapmaprs4889009
1000 genomesrs4889009
hgdprs4889009
ensemblrs4889009
gopubmedrs4889009
geneviewrs4889009
scholarrs4889009
googlers4889009
pharmgkbrs4889009
gwascentralrs4889009
openSNPrs4889009
23andMers4889009
23andMe allrs4889009
SNP Nexus

SNPshotrs4889009
SNPdbers4889009
MSV3drs4889009
GWAS Ctlgrs4889009
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 24586183OA-icon.png]
Trait Serum thyroid peroxidase antibody positivity
Title Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
Risk Allele G
P-val 3E-7
Odds Ratio 1.14 [1.08-1.21]

[PMID 25683181] Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease