{{Rsnum
|rsid=398122876
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NFIX
|position=13075672
|Gene_s=NFIX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=19
|CLNACC=RCV000030644.24; RCV000030645.20
|CLNALLE=1; 2
|CLNDBN=Marshall-Smith syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265211:602535:561:73284007
|CLNHGVS=NC_000019.9:g.13186486G>A; NC_000019.9:g.13186486G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164005.0009; 164005.0010
|Disease=Marshall-Smith syndrome
|FwdALT=A,T
|FwdREF=G
|GENEINFO=NFIX:4784
|GENE_ID=4784
|GENE_NAME=NFIX
|REF=G
|RSPOS=13186486
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122876
}}