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rs6759952

From SNPedia

Orientationplus
Stabilizedplus
Make rs6759952(C;C)
Make rs6759952(C;T)
Make rs6759952(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position217406996
GeneDIRC3
is asnp
is mentioned by
dbSNPrs6759952
dbSNP (classic)rs6759952
ClinGenrs6759952
ebirs6759952
HLIrs6759952
Exacrs6759952
Gnomadrs6759952
Varsomers6759952
LitVarrs6759952
Maprs6759952
PheGenIrs6759952
Biobankrs6759952
1000 genomesrs6759952
hgdprs6759952
ensemblrs6759952
geneviewrs6759952
scholarrs6759952
googlers6759952
pharmgkbrs6759952
gwascentralrs6759952
openSNPrs6759952
23andMers6759952
SNPshotrs6759952
SNPdbers6759952
MSV3drs6759952
GWAS Ctlgrs6759952
GMAF0.4082
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23894154]
Trait Thyroid cancer
Title Genome-wide association study on differentiated thyroid cancer.
Risk Allele T
P-val 6E-10
Odds Ratio 1.25 [1.16-1.34]