{{Rsnum
|rsid=386833492
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A2
|position=149960981
|Gene_s=SLC26A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=5
|CLNACC=RCV000049420.2
|CLNALLE=1
|CLNDBN=Diastrophic dysplasia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1350:C0220726:222600:628:58561002
|CLNHGVS=NC_000005.9:g.149340544T>C
|CLNSIG=5
|Disease=Diastrophic dysplasia
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=149340544
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833492
|CLNSRC=GeneReviews
|CLNSRCID=NBK1350
|GENEINFO=SLC26A2:1836
|GENE_ID=1836
|GENE_NAME=SLC26A2
}}{{PMID Auto
|PMID=10482955
|Title=Identification of the Finnish founder mutation for diastrophic dysplasia (DTD).
}}

{{PMID Auto
|PMID=21077202
|Title=Genotype-phenotype correlation in DTDST dysplasias: Atelosteogenesis type II and diastrophic dysplasia variant in one family.
}}