{{Rsnum
|rsid=118204044
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MMADHC
|position=149570089
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MMADHC
}}{{omim
|id=611935
|rsnum=118204044
|variant=0001
}}{{ClinVar
|rsid=118204044
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=150426603
|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.150426603A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611935.0001
|CLNSIG=5
|CLNCUI=C1848553
|CLNDBN=Homocystinuria, cblD type, variant 1
|Disease=Homocystinuria
|CLNACC=RCV000000797.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1848553
}}