{{Rsnum
|rsid=137853069
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNJ10
|position=160042042
|Gene_s=KCNJ10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=602208
|variant=0004
|rsnum=137853069
}}{{ClinVar
|rsid=137853069
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=160042042
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=KCNJ10:3766
|GENE_NAME=KCNJ10
|GENE_ID=3766
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.160042042G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_002241.4:c.491C>T; 602208.0004
|CLNSIG=5
|CLNCUI=C2748572
|CLNDBN=SeSAME syndrome
|Disease=SeSAME syndrome
|CLNACC=RCV000007891.2
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2748572:612780:ORPHA199343
}}