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rs4731426

From SNPedia

Orientationplus
Stabilizedplus
Make rs4731426(C;C)
Make rs4731426(C;G)
Make rs4731426(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position128242017
GeneLEP
is asnp
is mentioned by
dbSNPrs4731426
ebirs4731426
HLIrs4731426
Exacrs4731426
Varsomers4731426
Maprs4731426
PheGenIrs4731426
hapmaprs4731426
1000 genomesrs4731426
hgdprs4731426
ensemblrs4731426
gopubmedrs4731426
geneviewrs4731426
scholarrs4731426
googlers4731426
pharmgkbrs4731426
gwascentralrs4731426
openSNPrs4731426
23andMers4731426
23andMe allrs4731426
SNP Nexus

SNPshotrs4731426
SNPdbers4731426
MSV3drs4731426
GWAS Ctlgrs4731426
GMAF0.4931
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19623271OA-icon.png] A Bayesian hierarchical model for analysis of SNP diversity in multilocus, multipopulation samples.


[PMID 21042325] Phenotypic and genetic variation in leptin as determinants of weight regain.


GET Evidence
rs4731426
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.453125
summary



[PMID 26167411] Genetic variants in leptin: Determinants of obesity and leptin levels in South Indian population