{{Rsnum
|rsid=104893919
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A2
|position=149978184
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A2
}}{{omim
|id=606718
|rsnum=104893919
|variant=0005
}}{{ClinVar
|rsid=104893919
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=149357747
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC26A2:1836
|GENE_NAME=SLC26A2
|GENE_ID=1836
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.149357747C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1350; 606718.0005
|CLNSIG=5
|CLNCUI=C0220726; C0265274
|CLNDBN=Diastrophic dysplasia; Achondrogenesis, type IB
|Disease=Diastrophic dysplasia; Achondrogenesis
|CLNACC=RCV000004310.2; RCV000023568.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1350:C0220726:222600:628:58561002; NBK1516:C0265274:600972:932:93298:14870002
}}