{{Rsnum
|rsid=119103222
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MCCC2
|position=70898448
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=609014
|rsnum=119103222
|variant=0005
}}{{ClinVar
|ALT=C
|CHROM=5
|CLNACC=RCV000002000.1
|CLNALLE=1
|CLNDBN=3-methylcrotonyl CoA carboxylase 2 deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1134:C1859499:210210:6
|CLNHGVS=NC_000005.9:g.70898448T>C
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609014.0005
|Disease=3-methylcrotonyl CoA carboxylase 2 deficiency
|FwdALT=C
|FwdREF=T
|GENEINFO=MCCC2:64087
|GENE_ID=64087
|GENE_NAME=MCCC2
|REF=T
|RSPOS=70898448
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=119103222
}}