rs77600076
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs77600076(A;C) |
Make rs77600076(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 18159125 |
Gene | CHODL |
is a | snp |
is | mentioned by |
dbSNP | rs77600076 |
dbSNP (classic) | rs77600076 |
ClinGen | rs77600076 |
ebi | rs77600076 |
HLI | rs77600076 |
Exac | rs77600076 |
Gnomad | rs77600076 |
Varsome | rs77600076 |
LitVar | rs77600076 |
Map | rs77600076 |
PheGenI | rs77600076 |
Biobank | rs77600076 |
1000 genomes | rs77600076 |
hgdp | rs77600076 |
ensembl | rs77600076 |
geneview | rs77600076 |
scholar | rs77600076 |
rs77600076 | |
pharmgkb | rs77600076 |
gwascentral | rs77600076 |
openSNP | rs77600076 |
23andMe | rs77600076 |
SNPshot | rs77600076 |
SNPdbe | rs77600076 |
MSV3d | rs77600076 |
GWAS Ctlg | rs77600076 |
GMAF | 0.01102 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Bulimia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | A |
P-val | 1E-6 |
Odds Ratio | .12 [0.075-0.173] unit decrease |