rs6593669
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6593669(C;C) |
Make rs6593669(C;T) |
Make rs6593669(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 95568926 |
is a | snp |
is | mentioned by |
dbSNP | rs6593669 |
dbSNP (classic) | rs6593669 |
ClinGen | rs6593669 |
ebi | rs6593669 |
HLI | rs6593669 |
Exac | rs6593669 |
Gnomad | rs6593669 |
Varsome | rs6593669 |
LitVar | rs6593669 |
Map | rs6593669 |
PheGenI | rs6593669 |
Biobank | rs6593669 |
1000 genomes | rs6593669 |
hgdp | rs6593669 |
ensembl | rs6593669 |
geneview | rs6593669 |
scholar | rs6593669 |
rs6593669 | |
pharmgkb | rs6593669 |
gwascentral | rs6593669 |
openSNP | rs6593669 |
23andMe | rs6593669 |
SNPshot | rs6593669 |
SNPdbe | rs6593669 |
MSV3d | rs6593669 |
GWAS Ctlg | rs6593669 |
GMAF | 0.331 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20054173] Genotype-phenotype associations in obesity dependent on definition of the obesity phenotype