{{Rsnum
|rsid=121908429
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC12A6
|position=34257713
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC12A6
}}{{omim
|id=604878
|rsnum=121908429
|variant=0008
}}{{ClinVar
|rsid=121908429
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=34549914
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC12A6:9990
|GENE_NAME=SLC12A6
|GENE_ID=9990
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.34549914G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604878.0008
|CLNSIG=5
|CLNCUI=C0795950
|CLNDBN=Andermann syndrome
|Disease=Andermann syndrome
|CLNACC=RCV000005657.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1372:C0795950:218000:1496
}}