{{Rsnum
|rsid=1801267
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DPYD
|position=97098598
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DPYD,DPYD-AS1
}}{{omim
|id=612779
|rsnum=1801267
|variant=0006
}}

{{ClinVar
|rsid=1801267
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=97098598
|CHROM=1
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050260080a15000502110100
|GENEINFO=DPYD-AS1:100873932; DPYD:1806
|GENE_NAME=DPYD-AS1; DPYD
|GENE_ID=100873932; 1806
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.97098598C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000110.3:c.2657G>A; NR_046590.1:n.64+2612C>T; 612779.0006
|CLNSIG=5
|CLNCUI=C2720286
|CLNDBN=Dihydropyrimidine dehydrogenase deficiency
|Disease=Dihydropyrimidine dehydrogenase deficiency
|CLNACC=RCV000000466.1
|Tags=RV;PM;S3D;NSM;REF;INT;OTH;ASP;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2720286:274270
}}

{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}