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rs2439302

From SNPedia

Orientationminus
Stabilizedminus
Make rs2439302(C;C)
Make rs2439302(C;G)
Make rs2439302(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position32574851
GeneNRG1
is asnp
is mentioned by
dbSNPrs2439302
dbSNP (classic)rs2439302
ClinGenrs2439302
ebirs2439302
HLIrs2439302
Exacrs2439302
Gnomadrs2439302
Varsomers2439302
LitVarrs2439302
Maprs2439302
PheGenIrs2439302
Biobankrs2439302
1000 genomesrs2439302
hgdprs2439302
ensemblrs2439302
geneviewrs2439302
scholarrs2439302
googlers2439302
pharmgkbrs2439302
gwascentralrs2439302
openSNPrs2439302
23andMers2439302
SNPshotrs2439302
SNPdbers2439302
MSV3drs2439302
GWAS Ctlgrs2439302
GMAF0.4013
Max Magnitude0
? (C;C) (C;G) (G;G) 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 G
P-val 2E-9
Odds Ratio 1.3600 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 25746573] Clinical significance of papillary thyroid cancer risk loci identified by genome-wide association studies


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


[PMID 28256518OA-icon.png] Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.


[PMID 29121253OA-icon.png] The role of NRG1 in the predisposition to papillary thyroid carcinoma.