{{Rsnum
|rsid=387907308
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NIN
|position=50744304
|Gene_s=NIN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000030830.1
|CLNALLE=1
|CLNDBN=Seckel syndrome 7
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN158704:614851
|CLNHGVS=NC_000014.8:g.51211022T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608684.0002
|Disease=Seckel syndrome 7
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=51211022
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907308
|GENEINFO=NIN:51199
|GENE_ID=51199
|GENE_NAME=NIN
}}