Rs116909374

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Orientationplus
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
Exacrs116909374
PheGenIrs116909374
nextbiors116909374
hapmaprs116909374
1000 genomesrs116909374
hgdprs116909374
ensemblrs116909374
gopubmedrs116909374
geneviewrs116909374
scholarrs116909374
googlers116909374
pharmgkbrs116909374
gwascentralrs116909374
openSNPrs116909374
23andMers116909374
23andMe allrs116909374
SNP Nexus

SNPshotrs116909374
SNPdbers116909374
MSV3drs116909374
GMAF0.01928
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 23659773] 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