{{Rsnum
|rsid=104894251
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=KCNJ1
|position=128839929
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ1
}}{{omim
|id=600359
|rsnum=104894251
|variant=0010
}}{{ClinVar
|rsid=104894251
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=128709824
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KCNJ1:3758
|GENE_NAME=KCNJ1
|GENE_ID=3758
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.128709824A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600359.0010
|CLNSIG=5
|CLNCUI=C1855849
|CLNDBN=Bartter syndrome antenatal type 2
|Disease=Bartter syndrome antenatal type 2
|CLNACC=RCV000009732.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1855849:241200
}}