{{Rsnum
|rsid=187464517
|Gene=NIN
|Chromosome=14
|position=50757365
|Orientation=plus
|GMAF=0.0009183
|Gene_s=NIN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=C
|CAF=0.9991; 0.0009183
|CHROM=14
|CLNACC=RCV000030829.1
|CLNALLE=1
|CLNDBN=Seckel syndrome 7
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN158704:614851
|CLNHGVS=NC_000014.8:g.51224083T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608684.0001
|COMMON=1
|Disease=Seckel syndrome 7
|FwdALT=C
|FwdREF=T
|GENEINFO=NIN:51199
|GENE_ID=51199
|GENE_NAME=NIN
|REF=T
|RSPOS=51224083
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000016110100
|WGT=0
|dbSNPBuildID=135
|rsid=187464517
}}