{{Rsnum
|rsid=137853061
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MTRR
|position=7892815
|Gene_s=MTRR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602568
|variant=0004
|rsnum=137853061
}}{{ClinVar
|rsid=137853061
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=7892928
|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.7892928G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602568.0004
|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=RCV000007446.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1328:C1856057:236270:2169:622
}}