{{Rsnum
|rsid=121913581
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MTR
|position=236897020
|Gene_s=MTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=156570
|rsnum=121913581
|variant=0010
}}{{ClinVar
|rsid=121913581
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=236897020
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=MTR:4548
|GENE_NAME=MTR
|GENE_ID=4548
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236897020G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000254.2:c.3613G>T; 156570.0010
|CLNSIG=5
|CLNCUI=C1855128
|CLNDBN=METHYLCOBALAMIN DEFICIENCY, cblG TYPE
|Disease=METHYLCOBALAMIN DEFICIENCY
|CLNACC=RCV000015357.25
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1328:C1855128:250940:ORPHA2170:ORPHA622
}}