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rs34079606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34079606(C;T)
Make rs34079606(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position54000500
GeneHOXC9
is asnp
is mentioned by
dbSNPrs34079606
ebirs34079606
HLIrs34079606
Exacrs34079606
Varsomers34079606
Maprs34079606
PheGenIrs34079606
hapmaprs34079606
1000 genomesrs34079606
hgdprs34079606
ensemblrs34079606
gopubmedrs34079606
geneviewrs34079606
scholarrs34079606
googlers34079606
pharmgkbrs34079606
gwascentralrs34079606
openSNPrs34079606
23andMers34079606
23andMe allrs34079606
SNP Nexus

SNPshotrs34079606
SNPdbers34079606
MSV3drs34079606
GWAS Ctlgrs34079606
GMAF0.01699
Max Magnitude0

[PMID 22106857OA-icon.png] Homeobox C9 Is Not Potentially Related to Congenital Heart Disease in Chinese Patients