{{Rsnum
|rsid=386833498
|Chromosome=5
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=SLC26A2
|position=149981317
|Gene_s=SLC26A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=5
|CLNACC=RCV000049426.1
|CLNALLE=1
|CLNDBN=Diastrophic dysplasia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1350:C0220726:222600:628:58561002
|CLNHGVS=NC_000005.9:g.149360880delA
|CLNSIG=4
|Disease=Diastrophic dysplasia
|FwdREF=A
|REF=TA
|RSPOS=149360878
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833498
|GENEINFO=SLC26A2:1836
|GENE_ID=1836
|GENE_NAME=SLC26A2
}}{{PMID Auto
|PMID=7923357
|Title=The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.
}}

{{PMID Auto
|PMID=8702127
|Title=A family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans.
}}

{{PMID Auto
|PMID=8723100
|Title=A chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations.
}}