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rs10028213

From SNPedia

Orientationplus
Stabilizedplus
Make rs10028213(C;C)
Make rs10028213(C;G)
Make rs10028213(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position148731458
is asnp
is mentioned by
dbSNPrs10028213
ebirs10028213
HLIrs10028213
Exacrs10028213
Varsomers10028213
Maprs10028213
PheGenIrs10028213
hapmaprs10028213
1000 genomesrs10028213
hgdprs10028213
ensemblrs10028213
gopubmedrs10028213
geneviewrs10028213
scholarrs10028213
googlers10028213
pharmgkbrs10028213
gwascentralrs10028213
openSNPrs10028213
23andMers10028213
23andMe allrs10028213
SNP Nexus

SNPshotrs10028213
SNPdbers10028213
MSV3drs10028213
GWAS Ctlgrs10028213
GMAF0.1837
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22494929]
Trait
Title Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.
Risk Allele C
P-val 3E-10
Odds Ratio 0.0840 None