{{Rsnum
|rsid=121908332
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNK9
|position=139618677
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNK9
}}{{omim
|id=605874
|rsnum=121908332
|variant=0001
}}{{ClinVar
|rsid=121908332
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=140630920
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a01000002110100
|GENEINFO=KCNK9:51305
|GENE_NAME=KCNK9
|GENE_ID=51305
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.140630920C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605874.0001
|CLNSIG=5
|CLNCUI=C2676770
|CLNDBN=Birk Barel mental retardation dysmorphism syndrome
|Disease=Birk Barel mental retardation dysmorphism syndrome
|CLNACC=RCV000005007.1
|Tags=RV;PM;S3D;NSM;REF;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2676770:612292:166108
}}