{{Rsnum
|rsid=6700896
|Gene=LEPR
|Chromosome=1
|position=65624099
|Orientation=plus
|GMAF=0.4591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LEPR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 42.3 | 45.9 | 11.7
| HCB | 0.0 | 20.9 | 79.1
| JPT | 0.9 | 19.5 | 79.6
| YRI | 23.3 | 52.7 | 24.0
| ASW | 32.1 | 33.9 | 33.9
| CHB | 0.0 | 20.9 | 79.1
| CHD | 0.9 | 22.0 | 77.1
| GIH | 29.0 | 50.0 | 21.0
| LWK | 34.3 | 53.7 | 12.0
| MEX | 21.4 | 42.9 | 35.7
| MKK | 39.4 | 47.1 | 13.5
| TSI | 39.2 | 46.1 | 14.7
| HapMapRevision=28
}}[http://blog.23andme.com/2009/06/30/genetic-study-casts-doubt-on-inflammatory-marker-as-cause-of-heart-disease/ 23andMe blog] [[rs6700896]](T) -14.8% lower CRP and associated with increased weight and body mass index

{{PMID Auto
|PMID=19567438
|Title=Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease
|OA=1
}}

{{PMID Auto
|PMID=22215535
|Title=Association of nonalcoholic fatty liver disease with a single nucleotide polymorphism on the gene encoding leptin receptor
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6700896
|overall_frequency_n=53
|overall_frequency_d=120
|overall_frequency=0.441667
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=53
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}