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rs9915657

From SNPedia

Orientationplus
Stabilizedplus
Make rs9915657(C;C)
Make rs9915657(C;T)
Make rs9915657(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position72131395
is asnp
is mentioned by
dbSNPrs9915657
dbSNP (classic)rs9915657
ClinGenrs9915657
ebirs9915657
HLIrs9915657
Exacrs9915657
Gnomadrs9915657
Varsomers9915657
LitVarrs9915657
Maprs9915657
PheGenIrs9915657
Biobankrs9915657
1000 genomesrs9915657
hgdprs9915657
ensemblrs9915657
geneviewrs9915657
scholarrs9915657
googlers9915657
pharmgkbrs9915657
gwascentralrs9915657
openSNPrs9915657
23andMers9915657
SNPshotrs9915657
SNPdbers9915657
MSV3drs9915657
GWAS Ctlgrs9915657
GMAF0.4408
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23408906OA-icon.png]
Trait Thyroid hormone levels
Title A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
Risk Allele T
P-val 8E-13
Odds Ratio .06 [0.046-0.082] unit decrease