{{Rsnum
|rsid=398122874
|Chromosome=19
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=NFIX
|position=13078651
|Gene_s=NFIX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=19
|CLNACC=RCV000030642.24
|CLNALLE=1
|CLNDBN=Marshall-Smith syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265211:602535:561:73284007
|CLNHGVS=NC_000019.9:g.13189465_13189466insT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164005.0007
|Disease=Marshall-Smith syndrome
|FwdALT=T
|GENEINFO=NFIX:4784
|GENE_ID=4784
|GENE_NAME=NFIX
|REF=C
|RSPOS=13189464
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398122874
}}