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rs10487506

From SNPedia

Orientationplus
Stabilizedplus
Make rs10487506(A;A)
Make rs10487506(A;G)
Make rs10487506(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position128238102
is asnp
is mentioned by
dbSNPrs10487506
ebirs10487506
HLIrs10487506
Exacrs10487506
Varsomers10487506
Maprs10487506
PheGenIrs10487506
hapmaprs10487506
1000 genomesrs10487506
hgdprs10487506
ensemblrs10487506
gopubmedrs10487506
geneviewrs10487506
scholarrs10487506
googlers10487506
pharmgkbrs10487506
gwascentralrs10487506
openSNPrs10487506
23andMers10487506
23andMe allrs10487506
SNP Nexus

SNPshotrs10487506
SNPdbers10487506
MSV3drs10487506
GWAS Ctlgrs10487506
GMAF0.4417
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23026132OA-icon.png] Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels


[PMID 23751306] Association between Leptin gene polymorphisms and plasma leptin level in three consanguinous families with obesity


[PMID 17903300OA-icon.png] Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.


[PMID 19623271OA-icon.png] A Bayesian hierarchical model for analysis of SNP diversity in multilocus, multipopulation samples.


[PMID 19942621OA-icon.png] An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6.