rs7532266
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7532266(A;A) |
Make rs7532266(A;C) |
Make rs7532266(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 23225130 |
is a | snp |
is | mentioned by |
dbSNP | rs7532266 |
dbSNP (classic) | rs7532266 |
ClinGen | rs7532266 |
ebi | rs7532266 |
HLI | rs7532266 |
Exac | rs7532266 |
Gnomad | rs7532266 |
Varsome | rs7532266 |
LitVar | rs7532266 |
Map | rs7532266 |
PheGenI | rs7532266 |
Biobank | rs7532266 |
1000 genomes | rs7532266 |
hgdp | rs7532266 |
ensembl | rs7532266 |
geneview | rs7532266 |
scholar | rs7532266 |
rs7532266 | |
pharmgkb | rs7532266 |
gwascentral | rs7532266 |
openSNP | rs7532266 |
23andMe | rs7532266 |
SNPshot | rs7532266 |
SNPdbe | rs7532266 |
MSV3d | rs7532266 |
GWAS Ctlg | rs7532266 |
GMAF | 0.314 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 21079607] A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa