{{Rsnum
|rsid=386833996
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC17A5
|position=73615443
|Gene_s=SLC17A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=6
|CLNACC=RCV000049973.1
|CLNALLE=1
|CLNDBN=Salla disease
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1470:C1096903:604369:834:87074006
|CLNHGVS=NC_000006.11:g.74325166C>T
|CLNSIG=4
|Disease=Salla disease
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=74325166
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833996
|GENEINFO=SLC17A5:26503
|GENE_ID=26503
|GENE_NAME=SLC17A5
}}{{PMID Auto
|PMID=15172005
|Title=A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred.
}}