{{Rsnum
|rsid=121918553
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=NUP62
|position=49908636
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IL4I1,NUP62
|Status=Merged
|Merged=121917865
}}{{omim
|id=605815
|rsnum=121918553
|variant=0001
}}{{ClinVar
|rsid=121918553
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=50411893
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050260080815000002110100
|GENEINFO=NUP62:23636; IL4I1:259307
|GENE_NAME=NUP62; IL4I1
|GENE_ID=23636; 259307
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.50411893T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605815.0001; 605815.0001
|CLNSIG=5
|CLNCUI=C0795996; C0795996
|CLNDBN=Striatonigral degeneration infantile
|Disease=Striatonigral degeneration infantile
|CLNACC=SCV000025194.1; SCV000025194.1
|Tags=RV;PM;S3D;NSM;INT;OTH;ASP;OTHERKG;LSD;OM
}}