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rs2295633

From SNPedia

Orientationminus
Stabilizedminus
Make rs2295633(C;C)
Make rs2295633(C;T)
Make rs2295633(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position46408711
GeneFAAH
is asnp
is mentioned by
dbSNPrs2295633
ebirs2295633
HLIrs2295633
Exacrs2295633
Varsomers2295633
Maprs2295633
PheGenIrs2295633
hapmaprs2295633
1000 genomesrs2295633
hgdprs2295633
ensemblrs2295633
gopubmedrs2295633
geneviewrs2295633
scholarrs2295633
googlers2295633
pharmgkbrs2295633
gwascentralrs2295633
openSNPrs2295633
23andMers2295633
23andMe allrs2295633
SNP Nexus

SNPshotrs2295633
SNPdbers2295633
MSV3drs2295633
GWAS Ctlgrs2295633
GMAF0.3535
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[PMID 22832737OA-icon.png] Fatty-acid amide hydrolase polymorphisms and post-traumatic stress disorder after penetrating brain injury


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


[PMID 19890266OA-icon.png] More aroused, less fatigued: fatty acid amide hydrolase gene polymorphisms influence acute response to amphetamine.


[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.