rs8046707
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8046707(A;A) |
Make rs8046707(A;G) |
Make rs8046707(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 30904912 |
is a | snp |
is | mentioned by |
dbSNP | rs8046707 |
dbSNP (classic) | rs8046707 |
ClinGen | rs8046707 |
ebi | rs8046707 |
HLI | rs8046707 |
Exac | rs8046707 |
Gnomad | rs8046707 |
Varsome | rs8046707 |
LitVar | rs8046707 |
Map | rs8046707 |
PheGenI | rs8046707 |
Biobank | rs8046707 |
1000 genomes | rs8046707 |
hgdp | rs8046707 |
ensembl | rs8046707 |
geneview | rs8046707 |
scholar | rs8046707 |
rs8046707 | |
pharmgkb | rs8046707 |
gwascentral | rs8046707 |
openSNP | rs8046707 |
23andMe | rs8046707 |
SNPshot | rs8046707 |
SNPdbe | rs8046707 |
MSV3d | rs8046707 |
GWAS Ctlg | rs8046707 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25025664] Common genetic variation in the human CTF1 locus, encoding cardiotrophin-1, determines insulin sensitivity