{{Rsnum
|rsid=118204048
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MMADHC
|position=149570117
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MMADHC
}}{{omim
|id=611935
|rsnum=118204048
|variant=0007
}}{{ClinVar
|rsid=118204048
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=150426631
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MMADHC:27249
|GENE_NAME=MMADHC
|GENE_ID=27249
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.150426631G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611935.0007
|CLNSIG=5
|CLNCUI=C1848552
|CLNDBN=Methylmalonic acidemia with homocystinuria cblD
|Disease=Methylmalonic acidemia with homocystinuria cblD
|CLNACC=RCV000000803.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1231:NBK1328:C1848552:277410:622:79283
}}