Have questions? Visit https://www.reddit.com/r/SNPedia

rs10917477

From SNPedia

Orientationplus
Stabilizedplus
Make rs10917477(A;A)
Make rs10917477(A;G)
Make rs10917477(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position19534612
is asnp
is mentioned by
dbSNPrs10917477
dbSNP (classic)rs10917477
ClinGenrs10917477
ebirs10917477
HLIrs10917477
Exacrs10917477
Gnomadrs10917477
Varsomers10917477
LitVarrs10917477
Maprs10917477
PheGenIrs10917477
Biobankrs10917477
1000 genomesrs10917477
hgdprs10917477
ensemblrs10917477
geneviewrs10917477
scholarrs10917477
googlers10917477
pharmgkbrs10917477
gwascentralrs10917477
openSNPrs10917477
23andMers10917477
SNPshotrs10917477
SNPdbers10917477
MSV3drs10917477
GWAS Ctlgrs10917477
GMAF0.3779
Max Magnitude0
? (A;A) (A;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 A
P-val 2E-8
Odds Ratio 0.0580 None