{{Rsnum
|rsid=121913666
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYCN
|position=15945847
|Gene_s=MYCN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=164840
|rsnum=121913666
|variant=0006
}}{{ClinVar
|rsid=121913666
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=16085969
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYCN:4613
|GENE_NAME=MYCN
|GENE_ID=4613
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.16085969G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164840.0006
|CLNSIG=5
|CLNCUI=C0796068
|CLNDBN=Feingold syndrome
|Disease=Feingold syndrome
|CLNACC=RCV000014912.20
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=NBK7050:C0796068:164280:602585:1305
}}