{{Rsnum
|rsid=104893915
|Gene=SLC26A2
|Chromosome=5
|position=149980428
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC26A2
}}{{omim
|id=606718
|rsnum=104893915
|variant=0002
}}{{ClinVar
|rsid=104893915
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=149359991
|CHROM=5
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=SLC26A2:1836
|GENE_NAME=SLC26A2
|GENE_ID=1836
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.149359991C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1350; 606718.0002
|CLNSIG=5
|CLNCUI=C1850554; C0220726; C1847593
|CLNDBN=Atelosteogenesis type 2; Diastrophic dysplasia; Multiple epiphyseal dysplasia 4
|Disease=Atelosteogenesis type 2; Diastrophic dysplasia; Multiple epiphyseal dysplasia 4
|CLNACC=RCV000004305.1; RCV000004306.2; RCV000004307.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1317:C1850554:256050:56304; NBK1350:C0220726:222600:628:58561002; NBK1306:C1847593:226900
|COMMON=0
}}