{{Rsnum
|rsid = 28936387
|Gene = SLC12A3
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=16
|position=56879153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC12A3
}}{{omim
|desc=GITELMAN SYNDROME
|id=600968
|rsnum=28936387
|variant=0002
}}

{{ClinVar
|rsid=28936387
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=56913065
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC12A3:6559
|GENE_NAME=SLC12A3
|GENE_ID=6559
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.56913065T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600968.0002
|CLNSIG=5
|CLNCUI=C0268450
|CLNDBN=Familial hypokalemia-hypomagnesemia
|Disease=Familial hypokalemia-hypomagnesemia
|CLNACC=RCV000009116.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268450:263800:358:3188003
}}

{{on chip | 23andMe v3}}