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rs8046707

From SNPedia

Orientationplus
Stabilizedplus
Make rs8046707(A;A)
Make rs8046707(A;G)
Make rs8046707(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position30904912
is asnp
is mentioned by
dbSNPrs8046707
ebirs8046707
HLIrs8046707
Exacrs8046707
Varsomers8046707
Maprs8046707
PheGenIrs8046707
hapmaprs8046707
1000 genomesrs8046707
hgdprs8046707
ensemblrs8046707
gopubmedrs8046707
geneviewrs8046707
scholarrs8046707
googlers8046707
pharmgkbrs8046707
gwascentralrs8046707
openSNPrs8046707
23andMers8046707
23andMe allrs8046707
SNP Nexus

SNPshotrs8046707
SNPdbers8046707
MSV3drs8046707
GWAS Ctlgrs8046707
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25025664OA-icon.png] Common genetic variation in the human CTF1 locus, encoding cardiotrophin-1, determines insulin sensitivity