rs2295632
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2295632(A;A) |
Make rs2295632(A;C) |
Make rs2295632(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 46413890 |
Gene | FAAH |
is a | snp |
is | mentioned by |
dbSNP | rs2295632 |
dbSNP (classic) | rs2295632 |
ClinGen | rs2295632 |
ebi | rs2295632 |
HLI | rs2295632 |
Exac | rs2295632 |
Gnomad | rs2295632 |
Varsome | rs2295632 |
LitVar | rs2295632 |
Map | rs2295632 |
PheGenI | rs2295632 |
Biobank | rs2295632 |
1000 genomes | rs2295632 |
hgdp | rs2295632 |
ensembl | rs2295632 |
geneview | rs2295632 |
scholar | rs2295632 |
rs2295632 | |
pharmgkb | rs2295632 |
gwascentral | rs2295632 |
openSNP | rs2295632 |
23andMe | rs2295632 |
SNPshot | rs2295632 |
SNPdbe | rs2295632 |
MSV3d | rs2295632 |
GWAS Ctlg | rs2295632 |
GMAF | 0.4298 |
Max Magnitude | 0 |
[PMID 20044928] Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity
[PMID 19014633] Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.
[PMID 20033240] Eating disorders: the current status of molecular genetic research.