{{Rsnum
|rsid=113994115
|Chromosome=2
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYCN
|position=15942281
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYCN,MYCNOS
}}{{omim
|id=164840
|rsnum=113994115
|variant=0004
}}{{ClinVar
|rsid=113994115
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=16082403
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=MYCN:4613; MYCNOS:10408
|GENE_NAME=MYCN; MYCNOS
|GENE_ID=4613; 10408
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.16082403G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK7050; 164840.0004
|CLNSIG=5
|CLNCUI=C0796068; C0796068
|CLNDBN=Feingold syndrome
|Disease=Feingold syndrome
|CLNACC=RCV000014910.24
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=NBK7050:C0796068:164280:602585:1305
}}