{{Rsnum
|rsid=45590836
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=1
|Orientation=minus
|Gene=MTHFR
|position=11791216
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MTHFR
}}{{omim
|id=607093
|desc=5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR
|rsnum=45590836
}}

{{omim
|id=607093
|rsnum=45590836
|variant=0010
}}

{{ClinVar
|rsid=45590836
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=11791216
|CHROM=1
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050178000a05000002110100
|GENEINFO=MTHFR:4524
|GENE_NAME=MTHFR
|GENE_ID=4524
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.11791216C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005957.4:c.1743G>A; 607093.0010
|CLNSIG=5
|CLNCUI=C1856058
|CLNDBN=Homocysteinemia due to MTHFR deficiency
|Disease=Homocysteinemia due to MTHFR deficiency
|CLNACC=RCV000003705.1
|Tags=RV;PM;TPA;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1856058:236250:ORPHA395
}}

{{PMID Auto
|PMID=19421414
|Title=Genetic variation in the methylenetetrahydrofolate reductase gene, MTHFR, does not alter the risk of visual failure in Leber's hereditary optic neuropathy.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}