rs74879986
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs74879986(A;A) |
Make rs74879986(A;G) |
Make rs74879986(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 31154556 |
is a | snp |
is | mentioned by |
dbSNP | rs74879986 |
dbSNP (classic) | rs74879986 |
ClinGen | rs74879986 |
ebi | rs74879986 |
HLI | rs74879986 |
Exac | rs74879986 |
Gnomad | rs74879986 |
Varsome | rs74879986 |
LitVar | rs74879986 |
Map | rs74879986 |
PheGenI | rs74879986 |
Biobank | rs74879986 |
1000 genomes | rs74879986 |
hgdp | rs74879986 |
ensembl | rs74879986 |
geneview | rs74879986 |
scholar | rs74879986 |
rs74879986 | |
pharmgkb | rs74879986 |
gwascentral | rs74879986 |
openSNP | rs74879986 |
23andMe | rs74879986 |
SNPshot | rs74879986 |
SNPdbe | rs74879986 |
MSV3d | rs74879986 |
GWAS Ctlg | rs74879986 |
GMAF | 0.01882 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Bulimia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | G |
P-val | 6E-6 |
Odds Ratio | .14 [0.079-0.201] unit decrease |