rs1556640
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1556640(C;C) |
Make rs1556640(C;T) |
Make rs1556640(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 138104895 |
Gene | PERP |
is a | snp |
is | mentioned by |
dbSNP | rs1556640 |
dbSNP (classic) | rs1556640 |
ClinGen | rs1556640 |
ebi | rs1556640 |
HLI | rs1556640 |
Exac | rs1556640 |
Gnomad | rs1556640 |
Varsome | rs1556640 |
LitVar | rs1556640 |
Map | rs1556640 |
PheGenI | rs1556640 |
Biobank | rs1556640 |
1000 genomes | rs1556640 |
hgdp | rs1556640 |
ensembl | rs1556640 |
geneview | rs1556640 |
scholar | rs1556640 |
rs1556640 | |
pharmgkb | rs1556640 |
gwascentral | rs1556640 |
openSNP | rs1556640 |
23andMe | rs1556640 |
SNPshot | rs1556640 |
SNPdbe | rs1556640 |
MSV3d | rs1556640 |
GWAS Ctlg | rs1556640 |
GMAF | 0.1878 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Bulimia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | T |
P-val | 2E-6 |
Odds Ratio | .08 [0.044-0.106] unit decrease |