rs10175070
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10175070(A;A) |
Make rs10175070(A;G) |
Make rs10175070(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 227805859 |
Gene | LRRC38 |
is a | snp |
is | mentioned by |
dbSNP | rs10175070 |
dbSNP (classic) | rs10175070 |
ClinGen | rs10175070 |
ebi | rs10175070 |
HLI | rs10175070 |
Exac | rs10175070 |
Gnomad | rs10175070 |
Varsome | rs10175070 |
LitVar | rs10175070 |
Map | rs10175070 |
PheGenI | rs10175070 |
Biobank | rs10175070 |
1000 genomes | rs10175070 |
hgdp | rs10175070 |
ensembl | rs10175070 |
geneview | rs10175070 |
scholar | rs10175070 |
rs10175070 | |
pharmgkb | rs10175070 |
gwascentral | rs10175070 |
openSNP | rs10175070 |
23andMe | rs10175070 |
SNPshot | rs10175070 |
SNPdbe | rs10175070 |
MSV3d | rs10175070 |
GWAS Ctlg | rs10175070 |
GMAF | 0.3503 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Eating disorders (purging via substances) |
Title | Genetic variants associated with disordered eating. |
Risk Allele | A |
P-val | 2E-6 |
Odds Ratio | .12 [0.073-0.175] unit increase |