{{Rsnum
|rsid=104894606
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NAGS
|position=44007772
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NAGS
}}{{omim
|id=608300
|rsnum=104894606
|variant=0007
}}{{ClinVar
|rsid=104894606
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=42085140
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NAGS:162417
|GENE_NAME=NAGS
|GENE_ID=162417
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.42085140T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608300.0007
|CLNSIG=5
|CLNCUI=C0268543
|CLNDBN=Hyperammonemia, type III
|Disease=Hyperammonemia
|CLNACC=RCV000002535.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268543:237310:927:57119000
}}