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rs13138932

From SNPedia

Orientationplus
Stabilizedplus
Make rs13138932(C;C)
Make rs13138932(C;T)
Make rs13138932(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position117962559
is asnp
is mentioned by
dbSNPrs13138932
ebirs13138932
HLIrs13138932
Exacrs13138932
Varsomers13138932
Maprs13138932
PheGenIrs13138932
hapmaprs13138932
1000 genomesrs13138932
hgdprs13138932
ensemblrs13138932
gopubmedrs13138932
geneviewrs13138932
scholarrs13138932
googlers13138932
pharmgkbrs13138932
gwascentralrs13138932
openSNPrs13138932
23andMers13138932
23andMe allrs13138932
SNP Nexus

SNPshotrs13138932
SNPdbers13138932
MSV3drs13138932
GWAS Ctlgrs13138932
GMAF0.2833
Max Magnitude

[PMID 23255945OA-icon.png] Polymorphisms in bone morphogenetic protein 3 and the risk of papillary thyroid cancer