{{Rsnum
|rsid=121913223
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=DHFR
|position=80633904
|Gene_s=DHFR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121913223
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=79929723
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=DHFR:1719
|GENE_NAME=DHFR
|GENE_ID=1719
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.79929723T>A
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=126060
|CLNDBN=Megaloblastic anemia due to dihydrofolate reductase deficiency
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000022525.22
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151205:613839
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=126060.0002
|Disease=Megaloblastic anemia due to dihydrofolate reductase deficiency
}}{{PMID Auto
|PMID=1060915
|Title=Dihydrofolate reductase deficiency causing megaloblastic anemia in two families.
}}

{{PMID Auto
|PMID=1099447
|Title=Inborn errors of folate metabolism (first of two parts).
}}

{{PMID Auto
|PMID=6700662
|Title=Hereditary abnormal transcobalamin II previously diagnosed as congenital dihydrofolate reductase deficiency.
}}
{{omim
|id=126060
|rsnum=121913223
}}