{{Rsnum
|rsid=121912591
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NAGS
|position=44006157
|Gene_s=NAGS,PYY
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608300
|rsnum=121912591
|variant=0005
}}{{ClinVar
|rsid=121912591
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=42083525
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PYY:5697; NAGS:162417
|GENE_NAME=PYY; NAGS
|GENE_ID=5697; 162417
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.42083525G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608300.0005
|CLNSIG=5
|CLNCUI=C0268543
|CLNDBN=Hyperammonemia, type III
|Disease=Hyperammonemia
|CLNACC=RCV000002533.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268543:237310:927:57119000
}}