rs1458201
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1458201(C;C) |
Make rs1458201(C;T) |
Make rs1458201(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 30904808 |
is a | snp |
is | mentioned by |
dbSNP | rs1458201 |
dbSNP (classic) | rs1458201 |
ClinGen | rs1458201 |
ebi | rs1458201 |
HLI | rs1458201 |
Exac | rs1458201 |
Gnomad | rs1458201 |
Varsome | rs1458201 |
LitVar | rs1458201 |
Map | rs1458201 |
PheGenI | rs1458201 |
Biobank | rs1458201 |
1000 genomes | rs1458201 |
hgdp | rs1458201 |
ensembl | rs1458201 |
geneview | rs1458201 |
scholar | rs1458201 |
rs1458201 | |
pharmgkb | rs1458201 |
gwascentral | rs1458201 |
openSNP | rs1458201 |
23andMe | rs1458201 |
SNPshot | rs1458201 |
SNPdbe | rs1458201 |
MSV3d | rs1458201 |
GWAS Ctlg | rs1458201 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25025664] Common genetic variation in the human CTF1 locus, encoding cardiotrophin-1, determines insulin sensitivity