{{Rsnum
|rsid=121913580
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MTR
|position=236852578
|Gene_s=MTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156570
|rsnum=121913580
|variant=0009
}}{{ClinVar
|rsid=121913580
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=236852578
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=MTR:4548
|GENE_NAME=MTR
|GENE_ID=4548
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236852578C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000254.2:c.1753C>T; 156570.0009
|CLNSIG=5
|CLNCUI=C1855128
|CLNDBN=METHYLCOBALAMIN DEFICIENCY, cblG TYPE
|Disease=METHYLCOBALAMIN DEFICIENCY
|CLNACC=RCV000015356.25
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1328:C1855128:250940:ORPHA2170:ORPHA622
}}