{{Rsnum
|rsid=121913582
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MTR
|position=236835586
|Gene_s=MTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156570
|rsnum=121913582
|variant=0011
}}{{ClinVar
|rsid=121913582
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=236835586
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060020a05000002110100
|GENEINFO=MTR:4548
|GENE_NAME=MTR
|GENE_ID=4548
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236835586G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000254.2:c.1228G>C; 156570.0011
|CLNSIG=5
|CLNCUI=C1855128
|CLNDBN=METHYLCOBALAMIN DEFICIENCY, cblG TYPE
|Disease=METHYLCOBALAMIN DEFICIENCY
|CLNACC=RCV000015358.25
|Tags=PM;NSM;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1328:C1855128:250940:ORPHA2170:ORPHA622
}}