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rs17767419

From SNPedia

Orientationplus
Stabilizedplus
Make rs17767419(C;C)
Make rs17767419(C;T)
Make rs17767419(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position79710651
is asnp
is mentioned by
dbSNPrs17767419
ebirs17767419
HLIrs17767419
Exacrs17767419
Varsomers17767419
Maprs17767419
PheGenIrs17767419
hapmaprs17767419
1000 genomesrs17767419
hgdprs17767419
ensemblrs17767419
gopubmedrs17767419
geneviewrs17767419
scholarrs17767419
googlers17767419
pharmgkbrs17767419
gwascentralrs17767419
openSNPrs17767419
23andMers17767419
23andMe allrs17767419
SNP Nexus

SNPshotrs17767419
SNPdbers17767419
MSV3drs17767419
GWAS Ctlgrs17767419
GMAF0.2778
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21565293OA-icon.png]
Trait
Title Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.
Risk Allele T
P-val 9E-15
Odds Ratio 0.0680 [0.05-0.09] unit increase