{{Rsnum
|rsid = 28940591
|Gene = PC
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=66871368
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PC
}}{{omim
|desc=PYRUVATE CARBOXYLASE DEFICIENCY
|id=608786
|rsnum=28940591
|variant=0003
}}

{{ population diversity
| geno1 = (C;T)
| geno2 = (T;T)
| geno3 = 
| CEU | 0 | 0 | 0
| HCB | 0 | 0 | 0
| JPT | 0 | 0 | 0
| YRI | 0 | 0 | 0
| ASW | 0 | 0 | 0
| CHD | 2.4 | 97.6 | 0
| GIH | 0 | 0 | 0
| LWK | 0 | 0 | 0
| MEX | 0 | 0 | 0
| MKK | 0 | 0 | 0
| TSI | 0 | 0 | 0
}}{{ClinVar
|rsid=28940591
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=66638839
|CHROM=11
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050160000000000402110100
|GENEINFO=PC:5091
|GENE_NAME=PC
|GENE_ID=5091
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.66638839A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1122; NBK6852; 608786.0003
|CLNSIG=5
|CLNCUI=C0034341; C0034341
|CLNDBN=Pyruvate carboxylase deficiency
|Disease=Pyruvate carboxylase deficiency
|CLNACC=RCV000002177.2
|Tags=RV;PM;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1122:NBK6852:C0034341:266150:3008:87694001
}}

{{on chip | 23andMe v1}}
{{on chip | Illumina Human 1M}}