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rs116909374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs116909374(C;T)
Make rs116909374(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position36269155
is asnp
is mentioned by
dbSNPrs116909374
dbSNP (classic)rs116909374
ClinGenrs116909374
ebirs116909374
HLIrs116909374
Exacrs116909374
Gnomadrs116909374
Varsomers116909374
LitVarrs116909374
Maprs116909374
PheGenIrs116909374
Biobankrs116909374
1000 genomesrs116909374
hgdprs116909374
ensemblrs116909374
geneviewrs116909374
scholarrs116909374
googlers116909374
pharmgkbrs116909374
gwascentralrs116909374
openSNPrs116909374
23andMers116909374
SNPshotrs116909374
SNPdbers116909374
MSV3drs116909374
GWAS Ctlgrs116909374
GMAF0.01928
Max Magnitude0
GWAS snp
PMID [PMID 22267200OA-icon.png]
Trait
Title Discovery of common variants associated with low TSH levels and thyroid cancer risk.
Risk Allele T
P-val 5E-11
Odds Ratio 2.0900 None

[PMID 23659773OA-icon.png] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma

[PMID 23847140] Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population

[PMID 24591304OA-icon.png] Significant SNPs have limited prediction ability for thyroid cancer

[PMID 26490305] Association Between GWAS-derived rs966423 Genetic Variant and Overall Mortality in Patients with Differentiated Thyroid Cancer


[PMID 31681970] Clinical implications of GWAS variants associated with differentiated thyroid cancer.