{{Rsnum
|rsid=121908077
|Chromosome=5
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GTT)
|geno3=(GTT;GTT)
|Gene=SLC26A2
|position=149980611
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A2
}}{{omim
|id=606718
|rsnum=121908077
|variant=0008
}}{{ClinVar
|rsid=121908077
|Reversed=0
|FwdREF=GTT
|FwdALT=
|REF=TGTT
|ALT=T
|RSPOS=149360167
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=SLC26A2:1836
|GENE_NAME=SLC26A2
|GENE_ID=1836
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.149360174_149360176delGTT
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1350; 606718.0008
|CLNSIG=5
|CLNCUI=C0265274
|CLNDBN=Achondrogenesis, type IB; Diastrophic dysplasia
|Disease=Achondrogenesis; Diastrophic dysplasia
|CLNACC=RCV000023571.1; RCV000055756.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1516:C0265274:600972:932:93298:14870002; NBK1350:C0220726:222600:628:58561002
}}