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Rs966423

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Orientationplus
Make rs966423(C;C)
Make rs966423(C;T)
Make rs966423(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position217445617
GeneDIRC3
is asnp
is mentioned by
dbSNPrs966423
PheGenIrs966423
nextbiors966423
hapmaprs966423
1000 genomesrs966423
hgdprs966423
ensemblrs966423
gopubmedrs966423
geneviewrs966423
scholarrs966423
googlers966423
pharmgkbrs966423
gwascentralrs966423
openSNPrs966423
23andMers966423
23andMe allrs966423
SNP Nexus

SNPshotrs966423
SNPdbers966423
MSV3drs966423
GMAF0.3696
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22267200OA-icon.png]
Trait
Title Discovery of common variants associated with low TSH levels and thyroid cancer risk.
Risk Allele C
P-val 1E-9
Odds Ratio 1.3400 None


[PMID 19481195OA-icon.png] The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.


[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 24591304] Significant SNPs have limited prediction ability for thyroid cancer