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rs12983047

From SNPedia

Orientationplus
Stabilizedplus
Make rs12983047(A;A)
Make rs12983047(A;G)
Make rs12983047(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position41328594
is asnp
is mentioned by
dbSNPrs12983047
dbSNP (classic)rs12983047
ClinGenrs12983047
ebirs12983047
HLIrs12983047
Exacrs12983047
Gnomadrs12983047
Varsomers12983047
LitVarrs12983047
Maprs12983047
PheGenIrs12983047
Biobankrs12983047
1000 genomesrs12983047
hgdprs12983047
ensemblrs12983047
geneviewrs12983047
scholarrs12983047
googlers12983047
pharmgkbrs12983047
gwascentralrs12983047
openSNPrs12983047
23andMers12983047
SNPshotrs12983047
SNPdbers12983047
MSV3drs12983047
GWAS Ctlgrs12983047
GMAF0.2351
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23059779] A Study of Ethnic Differences in TGFβ1 Gene Polymorphisms and Effects on the Risk of Radiation Pneumonitis in Non-Small-Cell Lung Cancer