{{Rsnum
|rsid = 28940590
|Gene = PC
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=11
|position=66850918
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PC
}}{{omim
|desc=PYRUVATE CARBOXYLASE DEFICIENCY
|id=608786
|rsnum=28940590
|variant=0002
}}

{{ClinVar
|rsid=28940590
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=66618389
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PC:5091
|GENE_NAME=PC
|GENE_ID=5091
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.66618389C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1122; NBK6852; 608786.0002
|CLNSIG=5
|CLNCUI=C0034341; C0034341
|CLNDBN=Pyruvate carboxylase deficiency
|Disease=Pyruvate carboxylase deficiency
|CLNACC=RCV000002176.2
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1122:NBK6852:C0034341:266150:3008:87694001
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}