{{Rsnum
|rsid=80338771
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SLC46A1
|position=28405258
|Gene_s=SLC46A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=17
|CLNACC=RCV000020950.1; RCV000059715.1
|CLNALLE=1
|CLNDBN=Congenital defect of folate absorption; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1673:C0342705:229050:90045:62578003
|CLNHGVS=NC_000017.10:g.26732276C>G
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; UniProtKB (variants)
|CLNSRCID=NBK1673; VAR_032826
|Disease=Congenital defect of folate absorption; not provided
|FwdALT=C
|FwdREF=G
|GENEINFO=SLC46A1:113235
|GENE_ID=113235
|GENE_NAME=SLC46A1
|REF=C
|RSPOS=26732276
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80338771
}}{{PMID Auto
|PMID=17446347
|Title=The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.
|OA=1
}}