{{Rsnum
|rsid=119103218
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MCCC1
|position=183037432
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MCCC1
}}{{omim
|id=609010
|rsnum=119103218
|variant=0007
}}{{ClinVar
|rsid=119103218
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=182755220
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MCCC1:56922
|GENE_NAME=MCCC1
|GENE_ID=56922
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.182755220A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609010.0007
|CLNSIG=5
|CLNCUI=CN028786
|CLNDBN=3 Methylcrotonyl-CoA carboxylase 1 deficiency
|Disease=3 Methylcrotonyl-CoA carboxylase 1 deficiency
|CLNACC=RCV000002012.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1134:CN028786:210200:6:124719001:13144005
}}