{{Rsnum
|rsid=397515391
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CC)
|geno3=(CC;CC)
|Gene=SLC46A1
|position=28405910
|Gene_s=SLC46A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=17
|CLNACC=RCV000023912.3
|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.26732928_26732929delGG
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1673; 611672.0009
|Disease=Congenital defect of folate absorption
|FwdREF=CC
|GENEINFO=SLC46A1:113235
|GENE_ID=113235
|GENE_NAME=SLC46A1
|REF=CGG
|RSPOS=26732927
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397515391
}}