{{Rsnum
|rsid=121909394
|Chromosome=20
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC4A11
|position=3228337
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC4A11
}}{{omim
|id=610206
|rsnum=121909394
|variant=0012
}}{{ClinVar
|rsid=121909394
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=3208983
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC4A11:83959
|GENE_NAME=SLC4A11
|GENE_ID=83959
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.3208983A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610206.0012
|CLNSIG=5
|CLNCUI=C1857572
|CLNDBN=Corneal dystrophy and perceptive deafness
|Disease=Corneal dystrophy and perceptive deafness
|CLNACC=RCV000001379.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857572:217400:1490
}}