{{Rsnum
|rsid=59172778
|Gene=KCNJ1
|Chromosome=11
|position=128839231
|Orientation=plus
|GMAF=0.005051
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KCNJ1
}}{{omim
|id=600359
|rsnum=59172778
|variant=0006
}}

{{ClinVar
|rsid=59172778
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=128709126
|CHROM=11
|GMAF=0.005
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050170000000040416110100
|GENEINFO=KCNJ1:3758
|GENE_NAME=KCNJ1
|GENE_ID=3758
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.128709126A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600359.0006
|CLNSIG=5
|CLNCUI=C1855849
|CLNDBN=Bartter syndrome antenatal type 2
|Disease=Bartter syndrome antenatal type 2
|CLNACC=RCV000009728.1
|Tags=PM;TPA;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9949; 0.005051
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1855849:241200
|COMMON=1
}}

{{GET Evidence
|gene=KCNJ1
|aa_change=Met357Thr
|aa_change_short=M357T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs59172778
|overall_frequency_n=68
|overall_frequency_d=10758
|overall_frequency=0.00632088
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.324
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}