{{Rsnum
|rsid=119103223
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MCCC2
|position=71632185
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MCCC2
}}{{omim
|id=609014
|rsnum=119103223
|variant=0006
}}{{ClinVar
|rsid=119103223
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=70928012
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MCCC2:64087
|GENE_NAME=MCCC2
|GENE_ID=64087
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.70928012G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609014.0006
|CLNSIG=5
|CLNCUI=C1859499
|CLNDBN=3-methylcrotonyl CoA carboxylase 2 deficiency
|Disease=3-methylcrotonyl CoA carboxylase 2 deficiency
|CLNACC=RCV000002001.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1134:C1859499:210210:6
}}