{{Rsnum
|rsid=121434347
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC6A19
|position=1213517
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC6A19
}}{{omim
|id=608893
|rsnum=121434347
|variant=0004
}}{{ClinVar
|rsid=121434347
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=1213632
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SLC6A19:340024
|GENE_NAME=SLC6A19
|GENE_ID=340024
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.1213632C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608893.0004
|CLNSIG=5
|CLNCUI=C0018609
|CLNDBN=Neutral 1 amino acid transport defect
|Disease=Neutral 1 amino acid transport defect
|CLNACC=RCV000002097.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0018609:234500:2116:80902009
}}