{{Rsnum
|rsid=386833505
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SLC26A2
|position=149977699
|Gene_s=SLC26A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=5
|CLNACC=RCV000049433.1
|CLNALLE=1
|CLNDBN=Diastrophic dysplasia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1350:C0220726:222600:628:58561002
|CLNHGVS=NC_000005.9:g.149357262C>G
|CLNSIG=4
|Disease=Diastrophic dysplasia
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=149357262
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833505
|GENEINFO=SLC26A2:1836
|GENE_ID=1836
|GENE_NAME=SLC26A2
}}{{PMID Auto
|PMID=11241838
|Title=Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 novel mutations, mutation review, associated skeletal phenotypes, and diagnostic relevance.
}}