{{Rsnum
|rsid=119103219
|Gene=MCCC2
|Chromosome=5
|position=70895499
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}
{{omim
|id=609014
|rsnum=119103219
|variant=0002
}}{{ClinVar
|ALT=C
|CAF=0.9991; 0.0009183
|CHROM=5
|CLNACC=RCV000001997.1; RCV000082095.1
|CLNALLE=1
|CLNDBN=3-methylcrotonyl CoA carboxylase 2 deficiency; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1134:C1859499:210210:6
|CLNHGVS=NC_000005.9:g.70895499G>C
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNSRCID=2189; 609014.0002
|COMMON=1
|Disease=3-methylcrotonyl CoA carboxylase 2 deficiency; not provided
|FwdALT=C
|FwdREF=G
|GENEINFO=MCCC2:64087
|GENE_ID=64087
|GENE_NAME=MCCC2
|REF=G
|RSPOS=70895499
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000016110100
|WGT=0
|dbSNPBuildID=132
|rsid=119103219
}}