{{Rsnum
|rsid=137853062
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MTRR
|position=7891405
|Gene_s=MTRR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602568
|variant=0007
|rsnum=137853062
}}{{ClinVar
|rsid=137853062
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=7891518
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MTRR:4552
|GENE_NAME=MTRR
|GENE_ID=4552
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.7891518C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602568.0007
|CLNSIG=5
|CLNCUI=C1856057
|CLNDBN=Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type
|Disease=Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism
|CLNACC=RCV000007449.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1328:C1856057:236270:2169:622
}}