{{Rsnum
|rsid=121918111
|Chromosome=2
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=POMC
|position=25161572
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POMC
}}{{omim
|id=176830
|rsnum=121918111
|variant=0001
}}{{ClinVar
|rsid=121918111
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=25384441
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=POMC:5443
|GENE_NAME=POMC
|GENE_ID=5443
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.25384441C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=176830.0001
|CLNSIG=5
|CLNCUI=C1857854
|CLNDBN=Proopiomelanocortin deficiency
|Disease=Proopiomelanocortin deficiency
|CLNACC=RCV000014281.23
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK174451:C1857854:609734:71526
}}