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rs324419

From SNPedia

Orientationminus
Stabilizedminus
Make rs324419(A;A)
Make rs324419(A;G)
Make rs324419(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position46406314
GeneFAAH
is asnp
is mentioned by
dbSNPrs324419
ebirs324419
HLIrs324419
Exacrs324419
Varsomers324419
Maprs324419
PheGenIrs324419
hapmaprs324419
1000 genomesrs324419
hgdprs324419
ensemblrs324419
gopubmedrs324419
geneviewrs324419
scholarrs324419
googlers324419
pharmgkbrs324419
gwascentralrs324419
openSNPrs324419
23andMers324419
23andMe allrs324419
SNP Nexus

SNPshotrs324419
SNPdbers324419
MSV3drs324419
GWAS Ctlgrs324419
GMAF0.08815
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20044928OA-icon.png] Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity


[PMID 22473870] Contribution of genetic variants to pain susceptibility in Parkinson disease


[PMID 17991615] Rapid screening for potentially relevant polymorphisms in the human fatty acid amide hydrolase gene using Pyrosequencing.


[PMID 19014633OA-icon.png] Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.


[PMID 20033240OA-icon.png] Eating disorders: the current status of molecular genetic research.


[PMID 20054193] Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population.


[PMID 21423693OA-icon.png] Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.