{{Rsnum
|rsid=154623632
|Chromosome=17
|Orientation=minus
|geno1=(AA;AA)
|geno2=(AA;GC)
|geno3=(GC;GC)
|Gene=SLC46A1
|position=28405917
|Gene_s=SLC46A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TTT
|CHROM=17
|CLNACC=RCV000020949.1
|CLNALLE=1
|CLNDBN=Congenital defect of folate absorption
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1673:C0342705:229050:90045:62578003
|CLNHGVS=NC_000017.10:g.26732935_26732936delGCinsTT
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1673
|Disease=Congenital defect of folate absorption
|FwdALT=AA
|FwdREF=GC
|GENEINFO=SLC46A1:113235
|GENE_ID=113235
|GENE_NAME=SLC46A1
|REF=TGC
|RSPOS=26732934
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=MNV
|VP=0x050160000000000002110800
|WGT=0
|dbSNPBuildID=133
|rsid=154623632
}}