{{Rsnum
|rsid=267606887
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MTHFR
|position=11795158
|Gene_s=MTHFR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000003700.1
|CLNALLE=1
|CLNDBN=Homocystinuria due to MTHFR deficiency
|CLNDSDB=MedGen
|CLNDSDBID=CN068661
|CLNHGVS=NC_000001.11:g.11795158T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_005957.4:c.971A>G; 607093.0005
|Disease=Homocystinuria due to MTHFR deficiency
|FwdALT=G
|FwdREF=A
|GENEINFO=MTHFR:4524
|GENE_ID=4524
|GENE_NAME=MTHFR
|REF=T
|RSPOS=11795158
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267606887
|CLNORIGIN=1
}}