{{Rsnum
|rsid=121434346
|Gene=SLC6A19
|Chromosome=5
|position=1212338
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SLC6A19
}}{{omim
|id=608893
|rsnum=121434346
|variant=0003
}}{{ClinVar
|rsid=121434346
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=1212453
|CHROM=5
|GMAF=0.0018
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=SLC6A19:340024
|GENE_NAME=SLC6A19
|GENE_ID=340024
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.1212453G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608893.0003
|CLNSIG=5
|CLNCUI=C0018609
|CLNDBN=Neutral 1 amino acid transport defect
|Disease=Neutral 1 amino acid transport defect
|CLNACC=RCV000002096.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0018609:234500:2116:80902009
|COMMON=1
}}