{{Rsnum
|rsid=13447324
|Chromosome=18
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MC4R
|position=60372245
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MC4R
}}{{omim
|id=155541
|rsnum=13447324
|variant=0003
}}{{ClinVar
|rsid=13447324
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=58039478
|CHROM=18
|dbSNPBuildID=121
|SSR=0
|SAO=1
|VP=0x050068000000040102110100
|GENEINFO=MC4R:4160
|GENE_NAME=MC4R
|GENE_ID=4160
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.58039478G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=155541.0003
|CLNSIG=5
|CLNCUI=C0028754
|CLNDBN=Obesity
|Disease=Obesity
|CLNACC=RCV000015394.24
|Tags=RV;PM;PMC;VLD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0028754:601665:71529:414916001
}}{{PMID Auto
|PMID=16507
|Title=Formaldehyde formation as a metabolite of methoxyflurane.
}}

{{PMID Auto
|PMID=10199800
|Title=Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans.
}}

{{PMID Auto
|PMID=12499395
|Title=Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations.
}}

{{PMID Auto
|PMID=12646665
|Title=Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene.
}}

{{PMID Auto
|PMID=12851297
|Title=Molecular genetics of human obesity-associated MC4R mutations.
}}

{{PMID Auto
|PMID=12970296
|Title=Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.
}}