rs6606697
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6606697(A;A) |
Make rs6606697(A;G) |
Make rs6606697(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 109173915 |
Gene | ACACB |
is a | snp |
is | mentioned by |
dbSNP | rs6606697 |
dbSNP (classic) | rs6606697 |
ClinGen | rs6606697 |
ebi | rs6606697 |
HLI | rs6606697 |
Exac | rs6606697 |
Gnomad | rs6606697 |
Varsome | rs6606697 |
LitVar | rs6606697 |
Map | rs6606697 |
PheGenI | rs6606697 |
Biobank | rs6606697 |
1000 genomes | rs6606697 |
hgdp | rs6606697 |
ensembl | rs6606697 |
geneview | rs6606697 |
scholar | rs6606697 |
rs6606697 | |
pharmgkb | rs6606697 |
gwascentral | rs6606697 |
openSNP | rs6606697 |
23andMe | rs6606697 |
SNPshot | rs6606697 |
SNPdbe | rs6606697 |
MSV3d | rs6606697 |
GWAS Ctlg | rs6606697 |
GMAF | 0.4045 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20855566] ACC2 gene polymorphisms, metabolic syndrome and gene-nutrient interactions with dietary fat